Quality control and non-conformance management for regulated manufacturing (FDA 21 CFR 820, IATF 16949, AS9100): NCR lifecycle and disposition, 5-Why/Ishikawa/fault-tree/8D root cause analysis, CAPA systems, SPC interpretation, AQL sampling, and supplier quality audits. Use when investigating non-conformances, performing root cause analysis, managing CAPAs, interpreting SPC data, or handling supplier quality issues.
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