Audits and Compliance
Audits are where the gap between what your QMS says and what your team actually does becomes painfully visible. Whether the auditor is IATF, AS9100, ISO 9001, VDA 6.3, or a customer second party team, the rituals look similar, the findings look similar, and the prep work is rarely as ready as anyone claims. The guides in this topic cover the practical checklists, the clauses most commonly missed, and how to keep an audit ready posture without dedicating a person full time to staring at the document control system. Written for engineers who would rather pass an audit than perform one.
9 articles in this topic
Featured article
IATF 16949 Internal Audit Checklist: What Every Quality Engineer Needs to Know
A practical IATF 16949 internal audit checklist covering all major clauses, common findings, and tips for running audits that actually prepare you for certification.
Read the full guideAS9100
Aerospace QMS specifics where AS9100 diverges from automotive practice.
AS9102 Form 2 Product Accountability: The Materials, Special Processes, and Functional Testing Evidence That Has to Survive a Customer Reviewer
AS9102 Form 2 is the FAI form most often returned by a customer reviewer, and not because of the part. It is the supply chain map: every material spec, every special process, every functional test, with the supplier and the cert that proves it. A practitioner walkthrough of what each cell has to carry, the four kickback patterns that cost the most rework, and how to QA the form before the binder leaves your hands.
AS9100 Clause-by-Clause Audit Readiness: What Objective Evidence Each Requirement Wants Before the CB Walks In
An AS9100D readiness walkthrough by clause. What objective evidence each requirement expects, how the certification body actually verifies it, and the specific gaps that turn into minor and major findings during Stage 2 and surveillance audits.
AS9102 Partial FAI Re-accomplishment: When You Need One and What Has to Be in the Binder
AS9102 partial FAI re-accomplishment is the clause aerospace SQEs argue about most. A practical guide to Clause 4 triggers, the impact analysis a customer expects to see, what changes on Form 1, Form 2, and Form 3 when scope is partial, and how to keep the original FAI binder defensible through a revision.
Characteristic Accountability in AS9102: How to Balloon a Drawing So Form 3 Maps One to One
Characteristic accountability is where most AS9102 FAI packages get rejected. A practical guide to ballooning a drawing under Rev C, what counts as a characteristic, how GD&T and notes get numbered, and how to make Form 3 map one to one to the design record.
Counterfeit Parts Prevention: How AS5553, AS9100 Clause 8.1.4, and DFARS Fit Together
A practical guide to counterfeit parts prevention for aerospace and defense suppliers. How AS5553, AS9100D Clause 8.1.4, and DFARS 252.246-7007 connect, what a counterfeit avoidance system actually requires, the authorized distributor rule, GIDEP reporting, and AS6171 test methods.
AS9102 First Article Inspection: How Form 1, Form 2, and Form 3 Fit Together Under Rev C
A practical guide to the AS9102 First Article Inspection report under Rev C. Form 1 part accountability, Form 2 material and process verification, Form 3 dimensional results, when an FAI is required, how to handle re-accomplishment, and what changed from Rev B.
AS9100 Internal Audit Checklist: What Aerospace Quality Teams Need to Cover
A practical AS9100D internal audit checklist for aerospace quality engineers. Covers all clauses, the aerospace-specific adders to ISO 9001, common Rev D findings, and how AS9100 differs from AS9102 and NADCAP.
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