CFR section
21 CFR 111.525(b): What requirements apply to a returned dietary supplement that quality control personnel approve for reprocessing?
PART 111-CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS · Subpart N-Returned Dietary Supplements
Key facts
| Citation | 21 CFR 111.525(b) |
|---|---|
| Section | What requirements apply to a returned dietary supplement that quality control personnel approve for reprocessing? |
| Part | PART 111-CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS |
| Subpart | Subpart N-Returned Dietary Supplements |
| Subchapter | 21 CFR B Food |
| Product types cited | Food/Cosmetics |
| Regulation text (excerpt) | (b) Quality control personnel must approve or reject the release for distribution of any returned dietary supplement that is reprocessed. |
At a glance
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About CFR sections cited by the FDA
Title 21 of the Code of Federal Regulations contains the FDA's regulations, including current good manufacturing practice and quality system requirements that inspections cite.