FDA Inspection
PuroVite Inc.PuroVite Inc. – FDA Inspection, Dec 23, 2024
Record Details
This FDA Inspection record concerns PuroVite Inc., with an inspection on December 23, 2024, issued by the Florida District Office, covering foods & cosmetics.
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ID · 30faef25-5653-4979-b735-5cc6b9ce87e7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1244271
- FDA center
- Foods & Cosmetics
- Project area
- Food Composition, Standards, Labeling, and Economics
- Outcome
- Form 483 issued
FDA Citations
12- 21 CFR 111.75(a)(1)(i)Component - verify identity, dietary ingredient
- 21 CFR 111.70(d)Specifications - labels, packaging
- 21 CFR 111.70(e)Specifications - finished dietary supplement
- 21 CFR 111.25Equipment - follow written procedures
- 21 CFR 111.610(a)Records - available; FDA
- 21 CFR 111.160(d)(1)Labels - identify
- 21 CFR 111.570(b)Records - written procedures; product complaint
- 21 CFR 111.535(b)Make and keep records - equipment and utensils
- 21 CFR 111.205(a)Master manufacturing record - prepared
- 21 CFR 111.260Batch record - required information
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