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e-CFR data is current as of January 14, 2021 |
Title 21 → Chapter I → Subchapter B → Part 111 → Subpart K → §111.370 |
Title 21: Food and Drugs
PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
Subpart K—Production and Process Control System: Requirements for Manufacturing Operations
§111.370 What requirements apply to rejected dietary supplements?
You must clearly identify, hold, and control under a quarantine system for appropriate disposition any dietary supplement that is rejected and unsuitable for use in manufacturing, packaging, or labeling operations.