IATF 16949 - Expert Advice Community

Clarification on Laboratory Evaluation Requirements (IATF 16949)

In the context of IATF 16949 requirements, is a formal evaluation of external calibration and testing laboratories required in addition to verifying ISO/IEC 17025 accreditation? If yes, then the applicable evaluation criteria for labs may differ from those used for raw material suppliers and may impact the supplier’s overall performance rating.

Use of a Single Quality Manual for a Group with Multiple Subsidiaries

Can a corporate group composed of three subsidiaries, each with its own name and legal information, use a single Quality Manual for all entities?

IATF 16949 CERTIFICATION BODIES

IATF 16949 eğitimlerini alacağımız yerler Certification Body(Bureau Veritas, SGS, BSI) ya da Lead Auditor olmak zorunda mıdır? AIAG CORE TOOLS eğitimleri için de aynı zorunlulukar geçerli midir? Danışmanlık ve belgelendirme adı altında piyasada birçok kuruluş var olup bu eğitimleri veriyor. Buralardan alınan sertifikalar geçersiz mi olur? En temel haliyle IATF 16949 Temel Bilgilendirme, İç Denetçi ve Core Tools eğitim sertifikalarını veren yerlerde hangi yeterlilikler olmalıdır?

CQI 17

Hi experienced men

Could you please share me the CQI17 implement experiences, including: Checklist template, Procedure,...?

I'm learning to prepare it for IATF audit and certification.

Thanks and Best regards

FMEA new style

Is FMEA new style compulsary to implement for new projects, previously set up in FMEA <2016 but now transferred to a different company. Or can we continue on the previous set up old style FMEA and copy this after relocation of the product?

NPI project for IATF

I would like to know what would be on a list of deliverables for an NPI project in an IATF-certified organization

Controlled documents

According to IATF1649, if there are documents used to record test results that are used every day by Production Employees should these documents be Controlled Documents?

Identifying Controlled prints/documents

I was wondering if there's any specific way to identify controlled updated prints/documents per IATF ? Is using a stamp permitted?

Chapter 10.3 from IATF

Dear IATF assistant,

I have a question regarding chapter 10.3 from IATF

It was mentioned that the continuous improvement procedure should include risk analysis such as FMEA. i would like to understand how exactly
Does it means for example that for every improvement action, we should make FMEA update or that we should take FMEA as input to define the improvements area or other thing

I hope i can get clarification from you
Thank you in advance

4.4.1.2 Product Safety

I am having a problem understanding what this means exactly> Is it a requirement to have a full procedure or is it enough to just mention Procut Safety in the Manual?