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FDA Inspection 821844 — Inotiv Inc

Inotiv Inc — FEI 1000140135

The FDA completed an inspection of Inotiv Inc on March 8, 2013 in West Lafayette, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 8, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
West Lafayette, IN (United States)

Facility

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  • 1100971 (NAI Fri Jul 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1078296 (NAI Fri Dec 07 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1038421 (NAI Thu Jan 11 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 848016 (NAI Thu Sep 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources