Write up quality system audit findings against ISO 9001 or IATF 16949

Help me write up findings from an internal quality management system audit. Standard: [ISO 9001:2015 / IATF 16949:2016 / AS9100D / ISO 13485 / other] Area or process audited: [e.g. "receiving inspection", "production Line 3", "calibration"] My raw audit notes: [PASTE what I observed, records sampled, people interviewed] Audit criteria beyond the standard: [our procedures, customer-specific requirements] For each issue in my notes: 1. Decide whether it is a major nonconformity (a requirement not met at all, or a systemic failure, or risk of nonconforming product reaching the customer), a minor nonconformity (an isolated lapse), or an opportunity for improvement. Explain the grading in one line. 2. Write the finding in three parts: - Requirement: the clause number and what it requires, plus our own procedure reference [ADD procedure number]. - Evidence: exactly what was seen, with record IDs, dates, and sample sizes, factual and blame-free. - Statement of nonconformity: what is missing or not done. 3. Do not write the corrective action for the auditee; note what the root cause investigation should look at. Also check my notes for: - Findings that are opinions without evidence (tell me what evidence to collect). - Several findings with the same underlying cause that should be combined. - Good practices worth recording. Return: a findings table (No. | Clause | Grade | Finding | Evidence ref.), the full write-ups, and a short summary for management review. Only cite clauses you are confident apply, and mark any you are unsure of [CHECK CLAUSE]. Do not add evidence I didn't record.