FDA Inspection 1289246 — Supplement Manufacturing Partner Inc.

Supplement Manufacturing Partner Inc. — FEI 3034898672

The FDA completed an inspection of Supplement Manufacturing Partner Inc. on Oct 29, 2025 in Largo, FL. 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: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 29, 2025
Fiscal Year
2026
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Largo, FL (United States)

Citations

IDCFRDescription
2284721 CFR 111.70(e)Specifications - finished dietary supplement
2288821 CFR 111.210Master manufacturing record - record requirements

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.