FDA Inspection 638536 — Actavis Laboratories FL, Inc.

Actavis Laboratories FL, Inc. — FEI 3003937591

The FDA completed an inspection of Actavis Laboratories FL, Inc. on January 14, 2010 in Sunrise, FL. 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
January 14, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sunrise, FL (United States)