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. Subpart L - Production and Process Control System: Requirements for Packaging and Labeling Operations
  7. 21 CFR § 111.430
21 CFR § 111.430
Under this subpart L, what records must you make and keep?
June 25, 2020
CFR

(a) You must make and keep records required under this subpart L in accordance with subpart P of this part.

(b) You must make and keep records of the written procedures for packaging and labeling operations.

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§ 111.425 What requirements apply to a packaged and labeled dietary supplement that is rejected for distribution?

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