FDA Inspection 822740 — Actavis Inc.

Actavis Inc. — FEI 3009211379

The FDA completed an inspection of Actavis Inc. on Mar 15, 2013 in Morristown, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 15, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Morristown, NJ (United States)

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