FDA Inspection 943490 — Provimi North America, LLC

Provimi North America, LLC — FEI 1921541

The FDA completed an inspection of Provimi North America, LLC on Sep 9, 2015 in Fremont, NE. 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). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 9, 2015
Fiscal Year
2015
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Fremont, NE (United States)

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