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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 21—Food and Drugs
  4. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  5. SUBCHAPTER B—FOOD FOR HUMAN CONSUMPTION
  6. PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
  7. Subpart N—Returned Dietary Supplements

21 CFR Part 111 - Subpart N - Returned Dietary Supplements

  • CFR
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  1. § 111.503 What are the requirements under this subpart N for written procedures?
  2. § 111.510 What requirements apply when a returned dietary supplement is received?
  3. § 111.515 When must a returned dietary supplement be destroyed, or otherwise suitably disposed of?
  4. § 111.520 When may a returned dietary supplement be salvaged?
  5. § 111.525 What requirements apply to a returned dietary supplement that quality control personnel approve for reprocessing?
  6. § 111.530 When must an investigation be conducted of your manufacturing processes and other batches?
  7. § 111.535 Under this subpart N, what records must you make and keep?

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