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FDA Inspection 1083270 — Provimi North America, LLC

Provimi North America, LLC — FEI 1921541

The FDA completed an inspection of Provimi North America, LLC on March 8, 2019 in Fremont, NE. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Veterinary.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
March 8, 2019
Fiscal Year
2019
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Fremont, NE (United States)

Facility

Other inspections at this facility

  • 1167529 (NAI Fri Mar 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1111467 (NAI Thu Nov 07 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1068359 (NAI Wed Aug 29 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1020627 (VAI Mon Aug 07 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 943490 (VAI Wed Sep 09 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources