FDA Inspection 854136 — Actavis LLC

Actavis LLC — FEI 3009017204

The FDA completed an inspection of Actavis LLC on October 29, 2013 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
October 29, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Edison, NJ (United States)