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FDA Inspection 1037205 — American Laboratories Pharma, LLC

American Laboratories Pharma, LLC — FEI 1920841

The FDA completed an inspection of American Laboratories Pharma, LLC on December 1, 2017 in Omaha, 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
December 1, 2017
Fiscal Year
2018
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Omaha, NE (United States)

Facility

Other inspections at this facility

  • 1237967 (VAI Fri May 03 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1187283 (OAI Mon Oct 03 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 951530 (NAI Fri Sep 04 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 806926 (NAI Mon Nov 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 716816 (NAI Mon May 02 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources