FM-198 Q1_ISO 9001

Audit Report Revision: 8.0

Effective Date: 07/11/22

API MONOGRAM / APIQR PROGRAM

API Spec Q1 9th Edition and ISO 9001:2015
AUDIT REPORT

Scope of the document:

This audit report shall be used when auditing organization claiming conformity to API Spec Q1 9th Edition
as a Quality Management System. Also, it is applicable to those organizations that in addition to API Q1
are claiming conformity to ISO 9001:2015 and/or API product specifications included in the Monogram
Program.

Requirements specific to ISO 9001:2015 are highlighted with GRAY shading and they are not applicable
when conducting audits that do not include ISO 9001:2015 within the scope.

This report is not applicable to audits with a scope limited to ISO 9001:2015.

For audits including Monogram Licenses:

The designated API auditor shall fill out the relevant section of this document and all applicable FM-199
supplementary audit reports associated with the API product specifications under the scope of the audit.

For Surveillance and Recertification audits of APIQR and Dual Facilities:

An audit of the full quality management system must be performed. All sections of this report must be
completed.

For Surveillance Audits of Monogram-only Facilities:

Section headings with an asterisk (*) are the mandatory sections that must be filled out during
surveillance audits of Monogram-only facilities. Applicable FM-199 audit reports shall be filled out entirely.

The mandatory sections are:

1. Audit Information, Audit Scope & License Scope

2. Use of API Monogram, APIQR and ANAB Marks
3. Alternative Marking Agreement (AMA)
4. Product Realization (with the exception of 5.3 Risk Assessment and Management, 5.5
Contingency Planning and 5.11 Management of Change)
5. Internal Audit (API Spec Q1 clause 6.2.2)
6. Audit Summary, Audit Time Summary & Auditor Conclusion/Recommendation

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Audit Information*
Facility ID:
Audit ID:

Company Name/ Document any changes in the space below:

Facility Name:

Facility Address:

Primary Account
Manager(s):

Lead Auditor:
Audit Team Members:
Audit Start Date: Audit End Date:
Audit Type: Number of Employees Verified Number of
(per myCerts): Employees:
Duration: *Assigned Audit Days: *Actual Audit Days:

Justification: *Justification required if different from required audit days – Notify API of any changes and update Audit Plan

Shifts: Start Time End Time No. of Employees Audited? (Y/N)

Shift 1

Shift 2

Shift 3

Explanation (required for shifts not audited or if sum of employees does not equal verified number of employees):

Audit Scope*
API Spec Q1:9th ed. ISO 9001:2015

Audit Criteria: API Spec(s):

Other criteria:

License(s)/Certificate(s) Scope*
--Mark all changes to the scope on this section–
License Cert # Status Expiration Date

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Verification of Scope of Registration / Monogram License(s) and Exclusions

Verify each of the following: Select One: Finding #:

Yes – Scope is Accurate / Appropriate

Scope of Registration is accurate for the activities and
No – Mark all changes on registration scope above
processes performed by the facility.
N/A – No Certificates of Registration

Monogram – product scope of Monogram License is Yes

accurate for the activities and processes performed by No – Mark all changes on license scope above
the facility and facility has the manufacturing capability
for each product within the scope of the license(s). N/A – No Monogram License(s)

Exclusions taken are allowable, applicable and Yes – Exclusions, if any, are Accurate/Appropriate
justified. Document any discrepancies.
Note: Please see Advisory 6 for allowable Monogram No - Exclusions are not Accurate/Appropriate – Mark all
Program design exclusions. changes on the scope section above
Significant changes to the QMS since previous audit (if applicable):

Use of API Monogram, APIQR and ANAB Marks*

Control of the Application of the API Monogram (API Spec Q1, Annex A.5)
Requirements: Objective Evidence / Comments: Finding #:

Marking/monogramming procedure addresses all

requirements of Annex A.5, including application and
removal of the Monogram.
Identify evidence of implementation, if applicable.

API Monogram Marks sampled (on products, letterhead, business cards or any API Verify each of the following:
other medium): Spec:
Note: Identify the API Specification and observed evidence
Applied by licensee only

Includes mark and

license number
Applied to product at
licensed facility location

Verify conformance of the following requirements. Enter N/A if mark is not used. Verified Finding #:
APIQR Marks are only on correspondence, advertising, and promotional materials that are related to the
goods and services referenced in the scope of the Organization’s registration.

The APIQR / ANAB Mark has not been used on a product or product packaging, related documentation, or
in such a way as to suggest that APIQR / ANAB have certified or approved any product, process or service
of the registered organization.

The APIQR and ANAB Marks are used in conjunction with the organization’s name, location and
registration certificate numbers.

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The ANAB Mark is used in conjunction with the APIQR Mark, and the size of the ANAB Mark does not
exceed the size of the APIQR Mark.
The APIQR and ANAB Marks are reproduced:
1. in black, its original colors or the predominant color of the letterhead or printing,
2. on a clearly contrasting background, and
3. In a size which makes the mark’s features clearly distinguishable and without distortion of its dimensions.
If applicable - Upon written notification, the organization immediately ceased and desisted in the use of the
APIQR/ANAB Marks and/or API Monogram:
1) upon suspension or cancellation, or
2) In any manner that is determined misleading by API / APIQR.
Applicant organization – APIQR, ANAB Marks and/or API Monogram have not been identified in
promotional materials or other company documentation.

Additional comments:

Alternative Marking Agreement (AMA)*

Refer to FM-011 API Monogram Program Alternative Marking of Products License Agreement

AMA Locations – Identify all AMA locations and mark any changes

Scenarios applicable
(See FM-011, Table 1. Select all that apply) ☐Scenario 1 ☐Scenario 2 ☐Scenario 3

Requirement: Objective Evidence/Comments: Finding #

Scenarios 1 & 2 only:
• Subcontracted processes and API Monogram marking
planned and documented as part of QMS
• Maintains ownership of the product and sufficient
inspection procedures
• Processes and controls to verify conformance identified
• Subcontractor (Marking Party) is an authorized API
Marker
• Mill test reports or certificates of compliance issued by
either the Licensee or Marking Party include a statement
identifying that processing, product conformance
verification, and API Monogram application were
performed at the facility by an authorized API Marker
• Licensee remains responsible for all failures to meet the
API specification, through delivery of the final product
Scenario 3 only:
• Subdivision of bulk items and API Monogram marking
planned and documented as part of QMS
• Maintains ownership of the product and sufficient
inspection procedures
• Processes and controls to verify conformance identified
• Subcontractor (Marking Party) is an authorized API
Marker

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• Licensee remains responsible for all failures to meet the

API specification, through delivery of the final product

Quality Management System Requirements

In the space provided below, detail the objective evidence (documentation reviewed, records reviewed and personnel interviewed) to
ensure conformance to the identified QMS requirements. Detail any discrepancies / nonconformance identified.

API Spec Q1, Section 4.1 Quality Management System

Requirement: Objective Evidence/Comments: Finding #:

• QMS Scope
• Quality Manual
• QMS Processes
• Quality Policy
• Quality Objectives
• QMS Planning
• Internal and External Communication

• Organization and Context - ISO 9001, 4.1

• Interested Parties - ISO 9001, 4.2
• Scope of the QMS - ISO 9001, 4.3
• Policy strategic direction - ISO 9001, 5.2.1
• Policy availability - ISO 9001, 5.2.2
• Quality Objectives relevance - ISO 9001, 6.2.1
• Quality Objectives planning – ISO 9001, 6.2.2

API Spec Q1, Section 4.2 Management Responsibility

Requirement: Objective Evidence/Comments: Finding #:

• Availability of Resources
• Commitment to the QMS
• Responsibility and Authority
• Management Representative

• Leadership and Commitment – ISO 9001, 5.1.1

API Spec Q1, Section 4.3 Organizational Capability

Requirement: Objective Evidence/Comments: Finding #:

• Provision of resources
• Personnel Competence
• Training and Awareness
• Work Environment
• Resources / General – ISO 9001, 7.1.1
• Organizational Knowledge – ISO 9001, 7.1.6

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Personnel Sampled for Competency, Awareness and Training

Defined Competency Competency Records
Name Job Title Finding#:
Requirement(s)

• Defined Competency Requirement: Organization’s required qualification/competency requirements for the specific position.
• Competency Records: Sampled employee records (e.g. education, experience, certificate, training, etc.)

API Spec Q1, Section 4.4 Documentation Requirements

Requirement: Objective Evidence/Comments: Finding #:

• QMS Documentation
• Control of Documents
• Use of External Documents in Product
Realization. Ensure that all applicable official
API specifications and normative standards are
available for personnel to use. API
specifications must not be unauthorized
reproductions or altered versions.

Procedures required by API Spec Q1

Verify that procedures required by the standard are established, documented, implemented, and maintained for continual suitability.
(Please complete the Identification of QMS Procedures table and identify any nonconformities as applicable)

API Mark with API Mark with

Spec Q1 Requirement “X” if Finding# Spec Q1 Requirement “X” if Finding#
Clause available Clause available

4.3.2.1 Competency and Training 5.7.4 Product Inspection/Test

4.4.3 Control of Documents 5.7.5 Customer-supplied Property

4.4.4 Use of External Documents 5.7.6 Preservation of Product

4.5 Control of Records 5.7.7 Inspection & Testing

5.1.1 Review of Requirements 5.7.8 Preventive Maintenance

Risk Assessment & Control of Testing, Measuring, &

5.3 5.8
Management Monitoring Equipment

5.4.1 Design & Development 5.9 Product Release

5.10 Control of Nonconforming

5.5 Contingency Planning
Product

5.6 Purchasing 6.2.1 Customer Satisfaction

Verification of Purchased 6.2.2

5.6.3 Internal Audit
Products or Activities

5.7.1.1 Control of Production 6.3 Analysis of Data

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5.7.1.2 Control of Servicing 6.4.2 Corrective Action

Validation of Processes for 6.4.3

5.7.1.5 Preventive Action
Production and Servicing

5.7.3 Identification & Traceability Annex A Monogram Marking (if applicable)

API Spec Q1, Section 4.5 Control of Records

Requirement: Objective Evidence/Comments: Finding #:

• Controls include processes and responsibilities

for identification, collection, storage, protection,
retention, retrieval and disposition.
• Records are established and controlled to
provide evidence of conformity to requirements
and the QMS, including records originating
from outsourced activities.
• Records are maintained based on the required
retention times as specified in the applicable
standard, product spec, and / or the customer /
QMS requirements.
• Documented information – ISO 9001, 7.5.3.2

Product Realization*
Audit Conditions
Audit sampling priority should be established according to the conditions outlined below.
Category Category Definition
1 Monogram product currently being manufactured and available for review
Monogrammable (product meeting all requirements but not marked) product currently being
2
manufactured and available for review
3 Non-monogrammable product currently being manufactured and available for review
4 Monogram product manufactured since the last API audit but not available for review (records review)
Monogrammable product manufactured since the last API audit but not available for review (records
5
review)
Non-monogrammable product manufactured since the last API audit but not available for review
6
(records review)
Complete the table below based on the above classifications:
Category Product/Service Identification Specification (as applicable)

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In the space provided below, detail the objective evidence (documentation reviewed, records reviewed and personnel interviewed) to
ensure conformance to the identified QMS requirements. Detail any discrepancies / nonconformance identified.

API Spec Q1, Section 5.1 Contract Review *

List Contracts reviewed / sampled (Include contract number, customer name, date of API Spec / Product:
contract and any other pertinent details below):

Requirement: Objective Evidence/Comments: Finding #:

• Determination of Requirements
• Review of Requirements

API Spec Q1, Section 5.2 Planning *

Requirement: Objective Evidence/Comments: Finding #:

• Planning of Product Realization

• Output of Planning

API Spec Q1, Section 5.3 Risk Assessment and Management

Requirement: Objective Evidence/Comments: Finding #:

• Risk Assessment Procedure

• Impact on Delivery
• Impact on Quality of Product

• Actions to address risks and opportunities –

ISO 9001, 4.4.1, 5.1.2 and 6.1

API Spec Q1, Section 5.4 Design and Development *

Select all that apply:
Performed in-house Performed at a different location within the same organization
Outsourced Excluded (For Monogram licenses, confirm with Advisory 6)

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List design packages sampled / verified:

Select a representative sampling of the applicable products (API Specifications and/or Scope of Registration)
• Any Monogram license in “Applicant” status requires verification of all product designs within the application scope.
• Any newly added product requires verification of design, if design is required.

Design Package Verify that the licensee/applicant has all required design packages available for each product under the
Requirements (Annex scope of each Monogram License (Yes/No. If no, provide details/identify NC):
A, A.6 – Monogram
Only)

Requirement: Objective Evidence/Comments: Finding #:

• Planning
• Inputs
• Outputs
• Review
• Verification and Final Review
• Validation and Approval
• Changes
• Controls over outsourcing

• D&D Planning – ISO 9001, 8.3.2

• Consequences of failure – ISO 9001, 8.3.3e

API Spec Q1, Section 5.5 Contingency Planning

Requirements: Objective Evidence / Comments: Finding #:

• Contingency planning based on assessed risk

• Contingency planning output

API Spec Q1, Section 5.6 Purchasing *

Requirements: Objective Evidence / Comments: Finding #:

• Purchasing Control
o Procedure
o Initial Supplier Evaluation – Critical
Purchases
o Initial Supplier Evaluation – Noncritical
Purchases
o Supplier Reevaluation
o Supplier Evaluation – Records
o Outsourcing
• Purchasing Information
• Verification of purchased products and

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activities

• External providers – ISO 9001, 8.4.3d & e

Suppliers Sampled – Critical

Product / Component / Activity Performed:
Purchases:

Suppliers Sampled – Noncritical

Product / Component / Activity Performed:
Purchases:

List all outsourced activities and processes (if applicable):

API Spec Q1, Section 5.7 Production and Servicing Provision *

Description of Production/Service Capabilities
• Describe the organization’s capability, including available machinery and test equipment, required for manufacturing
of products within the scope of certification.
• Identify products, monogrammable and nonmonogrammable, the organization is capable of providing.

Description of Production and/or Service Processes (describe what manufacturing/service processes take place at the
facility and interactions):
Processes must be described in specific detail to provide information regarding the capabilities of the facility being audited.
For example: machining > fit-up > welding > heat treatment > ultrasonic testing > assembly > hydrotest, etc.

Production and Servicing Processes reviewed / sampled:

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Personnel Work Inspection Process control

Product/service/
Process/Area: interviewed: Product/Service: status
Instruction part identified? documents:
(Name and position) identified?

Control of Production and Servicing Finding

Objective Evidence / Comments: #:
Requirements:

• Production

• Servicing

• Process Control Documents

• Product Realization Capability Documentation

• Prevention of human error – ISO 9001, 8.5.1g

• Post-delivery activities – ISO 9001, 8.5.5

API Spec Q1, Section 5.7.1.5 Validation of Processes for Production and Servicing *
Records reviewed for processes requiring validation (Y/N/NA) (select all that apply):
NDE Welding Heat Treatment Coating and Plating Other
Personnel Qualification WPS / PQR Personnel Qualification Personnel Qualification

Equipment Qualification WPQ Procedure/Wis Procedure/Wis

Work Environment Welder Continuity Log Furnace Surveys Equipment

Procedure Qualification Personnel Qualification Work Environment

Equipment Qualification

Finding
Requirements: Objective Evidence / Comments: #:

• Procedure
• Equipment
• Personnel
• Specific Methods
• Acceptance Criteria
• Records
• Revalidation

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API Spec Q1, Section 5.7 Production and Servicing Provision *

Requirements: Objective Evidence / Comments: Finding #:

• Product Quality Plans

• Identification and Traceability

• Product Inspection / Test Status

• Customer – supplied Property

• Preservation of Product
o Storage and Assessment

• Inspection and Testing

o In-process Inspection and Testing
o Final Inspection and Testing

• Preventive Maintenance

• External provider property – ISO 9001, 8.5.3

API Spec Q1, Section 5.8 Control of Testing, Measuring and Monitoring Equipment *
Requirements: Objective Evidence / Comments: Finding #:

Organization shall determine the testing,

monitoring, and measurement requirements and
the associated equipment needed to provide
evidence of conformity to those requirements.

Equipment and resources suitable for specific

testing, monitoring and measuring activities.
Controls established and implemented to ensure
that equipment is identified, calibrated,
maintained, and used in a manner consistent
with requirements.

Equipment observed / sampled (minimum of 3):

Note: Ensure that all inspection and testing requirements of the applicable product specification are addressed
Equipment
Description Frequency Due Date
Unique ID

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API Spec Q1, Section 5.9 Product Release *

Requirements: Objective Evidence / Comments: Finding #:

• Procedure
• Release upon satisfactory completion of
planned arrangements
• Identification of individual releasing product
• Records maintained

API Spec Q1, Section 5.10 Control of Nonconforming Product *

Requirements: Objective Evidence / Comments: Finding #:

• Procedure
• Method of addressing nonconforming product
• Release of nonconforming product under
concession
• Customer notification
• Records

Management of Change
API Spec Q1, Section 5.11 Management of Change
Requirements: Objective Evidence / Comments: Finding #:

• Potential risks identified

• MOC Process Implementation
o Changes in the Organizational Structure
o Changes in Key or Essential Personnel
o Changes in Suppliers of critical
product/service
o Changes to MS Procedures
• MOC Notification

• Planning of changes – ISO 9001, 6.3

• Responsibilities and Authorities –ISO 9001,
5.3e

QMS Monitoring, Measurement, Analysis, and Improvement

In the space provided below, detail the objective evidence (documentation reviewed, records reviewed and personnel interviewed) to
ensure conformance to the identified QMS requirements. Detail any discrepancies / nonconformance identified.

API Spec Q1, Section 6.1 General

Requirements: Objective Evidence / Comments: Finding #:

• Monitoring, measurement, analysis, and

improvement processes needed to ensure
conformity to requirements are planned and
implemented.
• Determination of the applicable methods,
techniques of analysis of data and extent of use.

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API Spec Q1, Section 6.2 Monitoring, Measuring and Improving

Requirements: Objective Evidence / Comments: Finding #:

• Customer Satisfaction
• *Internal Audits:
o Requirements
o Performance & Frequency
o Review and Closure
• Process Evaluation

API Spec Q1, Section 6.3 Analysis of Data

Requirements: Objective Evidence / Comments: Finding #:

Analysis includes data generated from monitoring

& measurement, internal audits, management
reviews, and other relevant sources.

Analysis and Evaluation – ISO 9001, 9.1.3d,e

Data Analysis shall provide information relating to each of the following: (identify any other evidence of analysis of data, if applicable)

Method of Data Method of Actions (if

Data Types Objective/KPI Result
Collection Analysis needed)

Customer Satisfaction
Product Conformity
Nonconformities/ product
failures after delivery/use
Process trends and
characteristics
Supplier Performance
Quality Objectives

API Spec Q1, Section 6.4 Improvement

Requirements: Objective Evidence / Comments: Finding #:

• Organization shall continually improve the

effectiveness of the QMS
• Corrective Action
• Preventive Action
• Risks and opportunities update – ISO 9001,
10.2.1e

API Spec Q1, Section 6.5 Management Review

Finding #:
Requirements: Objective Evidence / Comments:

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• Management reviews are conducted at least

every 12 months.
• Input Requirements
• Output Requirements
• Management review inputs – ISO 9001, 9.3.2d,e

Audit Summary*
The API audit is based on a sampling process of the available information

Number of Findings: Major Nonconformities Minor Nonconformities

Concerns:
(Systemic): (Isolated):
Comments:

Strengths:

Opportunities for Improvement (OFIs):

Summary of the closure and verification of corrective actions for previous findings, if any:

Overall assessment of the capability of the facility to manufacture product(s) (Monogram), the effectiveness of the
management system, and the facility’s ability to perform activities/provide products within the scope of registration:

Were audit objectives achieved (Y/N)? Comments:

(See Audit Plan document for description of objectives. If audit objectives
were not achieved, provide detailed explanation and notify API immediately)

Were there significant deviations from the audit plan (Y/N)? Comments:
(If any deviations from audit plan, identify reasons and upload an as-
performed revision of the audit plan to myCerts)

Audit Time Summary*

Date Start Time End Time Facility Rep Initials
Day 1

Day 2

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Day 3

Day 4

Day 5

Day 6

Day 7
If audit duration is longer than 7 days, please add additional daily start/stop time.
Time spent auditing offsite or at other locations, such as subcontractors, must be identified and noted in the audit report.

Auditor Conclusion / Recommendation*

NOTE: API makes the final determination of certification status and shall be the sole
judge of whether licensing/registration will be granted/maintained

Registration and / or Licensing may be granted / continued / reinstated based on satisfactory implementation of a Management
System and / or demonstrated capability to meet applicable specification requirements with no nonconformities identified.*
Registration and / or Licensing may be granted / continued / reinstated subject to the review of the nonconformance(s)
identified and acceptance of appropriate corrective action(s) by the API Licensing and Registration Committee. *
Registration and / or Licensing may be subject to the review of the audit results and nonconformance(s) identified, acceptance
of appropriate corrective action(s) and additional actions as defined by the API Licensing & Registration Committee. This
decision may include a re-audit to verify the required corrective actions, withdrawal, suspension and or cancelation.*
* Note: Audits may result in suspension or cancellation of the organization’s license(s) and/or registration(s) or withdrawal of application
for licensing/registration. API makes the final determination of certification status and shall be the sole judge of whether
licensing/registration will be granted/maintained. You will be notified by API if your license/registration is adversely affected by the results
of this audit.
If any part of this audit was performed remotely, please specify (to be completed by Lead Auditor):
• Which processes were audited remotely?

• Whether the remote auditing techniques were effective in achieving the audit objectives?

• Areas that require special attention during the next on-site audit, if applicable. Please provide a detailed
explanation.

Final Auditor / Audit Team Remarks:

Organization’s Representative Comments:

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By signing below, I (we) attest that the information above is accurate and has been collected by the audit team during the
performance of the audit that was assigned to me (us) by API and that audit recommendations and conclusions were
communicated to the organization. (Digital Signatures are acceptable)
Audit Team Leader: Date:
Audit Team Member: Date:
Audit Team Member: Date:
By signing this document, it is not an admission of the acceptance of any nonconformities/concerns identified by the audit
team. The signature only confirms that the audit was performed and the audit recommendations and audit conclusions were
communicated by the auditor. API reserves the right to have final determination of the level of nonconformity identified in the
audit report. (Digital Signatures are acceptable)
Organization Representative (optional): Date:
Enter the next audit date below :
• Initial 1st Surveillance audit after stage 2 initial audit – 9 months after the last day of the initial stage 2 audit
• 1st surveillance audits – 30 months before expiration date
• 2nd surveillance audits – 18 months before expiration date
• Recertification/Renewal audits – 6 months before expiration date
Next Audit Target Date:
Next Audit Type:
(Preliminary date subject to change)

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Opening / Closing Meeting Attendance Sheet

When performing the opening and closing meeting, please refer to the Opening and Closing meeting guidelines
Facility ID: Audit ID:
Audit Team Leader:
Audit Team Members:
Audit Observer(s):
Opening Meeting Date: Time:
Closing Meeting
Date: Time:

Participants (Name & Position) - Initial/check the meetings attended Opening Closing

The information contained in this report is confidential and subject to the confidentiality agreement between the Audit
Team/Auditor(s) and API. Details of the assessment results are found in the succeeding pages of this report.

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