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  • IATF 16949 implementation

    I have few doubts in IATF implementation after discussions with OEMS:

    1. When MSA has to performed?
          After every calibration?
         Change of operators/ inspectors?
         When we have a large variety of parts or part numbers of various sizes, then how to perform MSA? For all part numbers?
    2. Is it necessary to mention Work instruction revision no. and date in PFMEA and Control plan?
    3. In PFMEA, each function/requirement has to be classified as minor, moderate, major or to mention only SC/CC wherever required?

    If you can please guide me on above topics.

  • TPM implementation

    I'm in the production process and I belong to the plant engineering and maintenance, and I'd like to know more about the TPM implementation, the kit mention in the document code 16 Procedure for Equipment Maintenance and Measuring Equipment, but I don't know if you have more information about how TPM should be implemented.

  • Operator observance audit

    May I know, operator observance audit covers in which clause?

  • IATF Document Hierarchy

    Per IATF requirements, is it acceptable to have the Manual, Policy, and Procedures all as Level I Documents? Looking at the Pyramid, it appears as though the Manual and Policy should be level I, and the procedures listed as level II, not combines as equal entities as Level I documents?

  • Product safety

    Hello. Product safety is something like Safety special characteristics? Thank you

  • Addressing TPM

    I have a question, I need to know what ISO 9001 and IATF 1699 documents/forms, etc... you have that address TPM. We are already ISO and IATF Certified, but this element of the standards has always been deficient and we want to make it a strength.

  • Internal auditor qualification

    Can our certified IATF 16949 internal auditor perform CQI-9 and/ or Nadcap heat treat audits? Based on IATF auditor training.

  • Customer specific requirement on Supplier Quality Assurance Manual

    Now, I get difficulties to find out what customer-specific requirement on Supplier Quality Assurance Manual besides Document or record retention and Symbol are given on Customer Drawing?
    Please help me with this by giving me a list of items on SQAM which need to be considered as CSR.

  • Applicable regulation in aftermarket

    My company is delivering actuators to an aftermarket equipment supplier which sells its products in XYZ. We don't have any requirements from this customer. Initially, our products are intended for home and building markets.

    1. Which regulation we are supposed to satisfy for this application?
    2. What is our legal responsibility in case of an accident or injuries of an end-user?
  • Exteranl standards for calibration lab equipment

    Are there minimum requirements for external standards for lab equipment controls (eg iso 9001, iso guide 34)

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