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FDA Inspection 1256490 — Actavis LLC

Actavis LLC — FEI 3009017204

The FDA completed an inspection of Actavis LLC on November 22, 2024 in Edison, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 22, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Edison, NJ (United States)

Facility

Other inspections at this facility

  • 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))
  • 978483 (VAI Thu Jul 07 2016 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