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  1. US law
  2. Federal (United States)
  3. Regulations
  4. Title 21 CFR — Food and Drugs
  5. Chapter I — FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  6. Part 117 — CURRENT GOOD MANUFACTURING PRACTICE, HAZARD ANALYSIS, AND RISK-BASED PREVENTIVE CONTROLS FOR HUMAN FOOD
  7. Subpart E — Withdrawal of a Qualified Facility Exemption

Federal (United States) · Regulations

Subpart E — Withdrawal of a Qualified Facility Exemption

12 sections

12 sections

  • 21 C.F.R. § 117.251Circumstances that may lead FDA to withdraw a qualified facility exemption.
  • 21 C.F.R. § 117.254Issuance of an order to withdraw a qualified facility exemption.
  • 21 C.F.R. § 117.257Contents of an order to withdraw a qualified facility exemption.
  • 21 C.F.R. § 117.260Compliance with, or appeal of, an order to withdraw a qualified facility exemption.
  • 21 C.F.R. § 117.264Procedure for submitting an appeal.
  • 21 C.F.R. § 117.267Procedure for requesting an informal hearing.
  • 21 C.F.R. § 117.270Requirements applicable to an informal hearing.
  • 21 C.F.R. § 117.274Presiding officer for an appeal and for an informal hearing.
  • 21 C.F.R. § 117.277Timeframe for issuing a decision on an appeal.
  • 21 C.F.R. § 117.280Revocation of an order to withdraw a qualified facility exemption.
  • 21 C.F.R. § 117.284Final agency action.
  • 21 C.F.R. § 117.287Reinstatement of a qualified facility exemption that was withdrawn.
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