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00040 CAPA Management

PPT: PPT-00040 REV01 CAPA Management

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  • 21 CFR Part 861: Procedures for Performance Standards Development
  • 21 CFR Part 860: Medical Device Classification
  • 21 CFR Part 830: Unique Device Identification
  • 21 CFR Part 822: Postmarket Surveillance
  • 21 CFR Part 821 Medical Device Tracking Requirements

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