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FDA Inspection 978483 — Actavis LLC

Actavis LLC — FEI 3009017204

The FDA completed an inspection of Actavis LLC on July 7, 2016 in Edison, NJ. 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
July 7, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Edison, NJ (United States)

Facility

Other inspections at this facility

  • 1256490 (NAI Fri Nov 22 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1100659 (NAI Thu Aug 08 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1050957 (VAI Mon May 07 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 854136 (NAI Tue Oct 29 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 764993 (NAI Fri Jan 27 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources