1. LawStack
  2. Title 21 - Food and Drugs
  3. Chapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  4. Subchapter B - FOOD FOR HUMAN CONSUMPTION
  5. Part 111 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
  6. 21 CFR Subpart O
21 CFR Subpart O
Product Complaints
June 25, 2020
§
111.553
What are the requirements under this subpart O for written procedures?
§
111.560
What requirements apply to the review and investigation of a product complaint?
§
111.570
Under this subpart O, what records must you make and keep?
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Subpart N Returned Dietary Supplements
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Subpart P Records and Recordkeeping

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