Statutes, codes, and regulations
Code of Federal Regulations
Title 21 - FOOD AND DRUGSChapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICESSubchapter B - FOOD FOR HUMAN CONSUMPTIONPart 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
Section 111.370 - What requirements apply to rejected dietary supplements?

21 C.F.R. § 111.370

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Current through September 30, 2024
Section 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.

21 C.F.R. § 111.370