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FDA Inspection 994679 — Actavis Elizabeth LLC

Actavis Elizabeth LLC — FEI 2211563

The FDA completed an inspection of Actavis Elizabeth LLC on December 5, 2016 in Elizabeth, 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
December 5, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Elizabeth, NJ (United States)

Facility

Other inspections at this facility

  • 1215838 (NAI Mon Jul 24 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1041770 (NAI Mon Feb 05 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1003801 (VAI Wed Feb 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 939866 (VAI Thu Aug 27 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 908911 (NAI Tue Dec 02 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources