FDA Inspection 1221519 — Provita Supplements Inc.

Provita Supplements Inc. — FEI 3013433722

The FDA completed an inspection of Provita Supplements Inc. on Oct 27, 2023 in Minnetonka, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Veterinary.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 27, 2023
Fiscal Year
2024
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Minnetonka, MN (United States)

Additional details

FSVP

Citations

IDCFRDescription
2240521 CFR 1.502(a)Develop FSVP
2241621 CFR 1.504(a)Hazard analysis written

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