FDA Inspection 822740 — Actavis Inc.

Actavis Inc. — FEI 3009211379

The FDA completed an inspection of Actavis Inc. on March 15, 2013 in Morristown, 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
March 15, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Morristown, NJ (United States)