FDA Inspection 1225332 — Biofarma US

Biofarma US — FEI 3013678210

The FDA completed an inspection of Biofarma US on Dec 18, 2023 in East Windsor, NJ. 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). 1 citation was issued during this inspection. Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 18, 2023
Fiscal Year
2024
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
East Windsor, NJ (United States)

Citations

IDCFRDescription
1576321 CFR 111.205(a)Master manufacturing record - unique formulation

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