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FDA Inspection 943490 — Provimi North America, LLC

Provimi North America, LLC — FEI 1921541

The FDA completed an inspection of Provimi North America, LLC on September 9, 2015 in Fremont, NE. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

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

Facility

Other inspections at this facility

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  • 1111467 (NAI Thu Nov 07 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1083270 (OAI Fri Mar 08 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))

FDA data resources