FDA Inspection
CLVM LLCCLVM LLC – FDA Inspection, Aug 1, 2025
Record Details
This FDA Inspection record concerns CLVM LLC, with an inspection on August 1, 2025, issued by the Denver District Office, covering foods & cosmetics.
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ID · 1ea7225c-c11c-42ed-adec-fcca5996d53b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1277111
- FDA center
- Foods & Cosmetics
- Project area
- Foodborne Biological Hazards
- Outcome
- Form 483 issued
FDA Citations
13- 21 CFR 108.25(c)(1)Registration
- 21 CFR 111.113(b)(2)Quality control - reject; specification not met
- 21 CFR 111.123(b)(2)Quality control - batch, product specifications
- 21 CFR 111.210Master manufacturing record - record requirements
- 21 CFR 111.260Batch record - required information
- 21 CFR 111.303Written procedures - establish; laboratory
- 21 CFR 111.453Written procedures - follow; holding and distribution
- 21 CFR 111.70(b)Specifications - components
- 21 CFR 111.70(e)Specifications - finished dietary supplement
- 21 CFR 111.75(a)(2)(ii)(B)Component - certificate of analysis
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