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    Non Conformity Format 01-10-2022

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    qc vahinipipes
    This document is a non-conformance report used to document any issues found with products during inspection activities. It contains sections to identify the non-conformance such as the product name and batch number, a description of what was found, and the proposed corrective actions. The report requires approval and signatures from quality and production personnel to document how the issue was addressed.

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    Download as PDF, TXT or read online from Scribd

    Non Conformity Format 01-10-2022

    Uploaded by

    qc vahinipipes
    136 views1 page
    This document is a non-conformance report used to document any issues found with products during inspection activities. It contains sections to identify the non-conformance such as the product name and batch number, a description of what was found, and the proposed corrective actions. The report requires approval and signatures from quality and production personnel to document how the issue was addressed.

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    This document is a non-conformance report used to document any issues found with products during inspection activities. It contains sections to identify the non-conformance such as the product name and batch number, a description of what was found, and the proposed corrective actions. The report requires approval and signatures from quality and production personnel to document how the issue was addressed.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    136 views1 page

    Non Conformity Format 01-10-2022

    Uploaded by

    qc vahinipipes
    This document is a non-conformance report used to document any issues found with products during inspection activities. It contains sections to identify the non-conformance such as the product name and batch number, a description of what was found, and the proposed corrective actions. The report requires approval and signatures from quality and production personnel to document how the issue was addressed.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    of 1

    Non-conformance Report

    Doc. No. : VIPL/QC/NC/22/10-01

    IDENTIFICATION
    1. Originator Name : 2. Date :
    3. Department : 4. NC No : DD/MM/Shift -No.

    5. Product Name/Type : 6. Quantity :


    7. Product Description : 8. Batch No :
    9. Shift and Time : 10. Machine No :

    11. Found during what activity :

    Final inspection Others

    Incoming inspection In process inspection

    12. Description of non-conformance (use continuation page if necessary)

    Cutter Man: Operator: Supervisor :

    13. Route Cause (use continuation page if necessary)

    Production Supervisor

    DISPOSITION
    14.
    Use as is Return to supplier
    Production Incharge
    Repair Reject Name:
    Reprocessing Date: Sign. :
    Justification if use as is /Repair:

    15. Approval Quality Incharge


    Non critical NC Name : Sign.
    Critical NC Date :

    CORRECTIVE/PREVENTIVE ACTION
    16. Description of proposed action (use continuation page if necessary)

    Quality Head: Production Head/Manager:


    Date Sign : Date Sign:

    CLOSING THE NON CONFORMANCE


    17. Planned disposition has been completed and corrective/preventive action has been initiated
    Responsible Manager Sign Date:

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