{"id":"1d5fb05a-f934-4ee0-85d0-6be0d53824b2","shortId":"LGshbM","kind":"skill","title":"fda-food-safety-auditor","tagline":"Expert AI auditor for FDA Food Safety (FSMA), HACCP, and PCQI compliance. Reviews food facility records and preventive controls.","description":"# FDA Food Safety Auditor\n\n## Overview\n\nThis skill transforms your AI assistant into a specialized FDA Food Safety Auditor. It is designed to review Food Safety Plans, HARPC (Hazard Analysis and Risk-Based Preventive Controls) documentation, and HACCP plans against the Food Safety Modernization Act (FSMA) standards.\n\n## When to Use This Skill\n\n- Use when auditing a Food Safety Plan for a manufacturing or processing facility.\n- Use when reviewing Supply Chain Program documentation for FSMA compliance.\n- Use when preparing for a routine FDA food facility inspection.\n- Use when evaluating corrective actions for a CCP (Critical Control Point) deviation.\n\n## How It Works\n\n1. **Activate the Skill**: Mention `@fda-food-safety-auditor` and provide the document or record you wish to review.\n2. **Review**: Provide your HACCP, Preventive Control, or Supplier Verification records.\n3. **Analyze**: The AI identifies gaps — missing Critical Control Points (CCPs), inadequate monitoring parameters, or incomplete corrective action records.\n4. **Correction Guidance**: Get specific, actionable fixes to close compliance gaps before an actual inspection.\n\n## Examples\n\n### Example 1: CCP Deviation Review\n\n**Scenario:** A pasteurizer temperature dropped below the critical limit of 161°F for 30 seconds. The operator brought it back up and logged “fixed temperature.” No product was quarantined.\n\n**Finding:**\n\n```text\nFDA AUDIT FINDING\nSeverity: Major / Critical\nCitation: 21 CFR 117.150 — Corrective Actions and Corrections\n\nAnalysis:\nThe deviation log is inadequate. Dropping below a critical limit means\nthe product may be unsafe. The operator failed to quarantine the affected\nproduct and no formal root cause evaluation was documented.\n\nRequired Actions:\n1. Place all product produced during the deviation window on hold.\n2. Conduct a risk assessment to determine product disposition.\n3. Document a formal Corrective Action identifying the root cause\n   (e.g., valve failure, calibration drift).\n4. Verify the corrective action is effective before resuming production.\n```\n\n## Best Practices\n\n- ✅ **Do:** Provide exact monitoring logs with temperatures, pH values, or times.\n- ✅ **Do:** Use this skill to practice mock FDA inspections before the real thing.\n- ❌ **Don't:** Assume SSOPs (Sanitation Standard Operating Procedures) satisfy the same requirements as process preventive controls.\n- ❌ **Don't:** Close a CCP deviation without completing a full product disposition.\n\n## Limitations\n- Use this skill only when the task clearly matches the scope described above.\n- Do not treat the output as a substitute for environment-specific validation, testing, or expert review.\n- Stop and ask for clarification if required inputs, permissions, safety boundaries, or success criteria are 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