FDA Inspection 1262868 — Pronuvia, Inc.

Pronuvia, Inc. — FEI 3012136993

The FDA completed an inspection of Pronuvia, Inc. on Feb 25, 2025 in Flushing, NY. 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). 5 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 25, 2025
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Flushing, NY (United States)

Citations

IDCFRDescription
1564221 CFR 111.455(a)Hold - temperature, humidity, light
1600021 CFR 111.130Quality control operations - returned dietary supplement
2281321 CFR 111.553Written procedures - establish; product complaint
2284721 CFR 111.70(e)Specifications - finished dietary supplement
2285921 CFR 111.103Written procedures - establish; quality control operations

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