FDA Inspection 996475 — Actavis Laboratories FL Inc.

Actavis Laboratories FL Inc. — FEI 3003937607

The FDA completed an inspection of Actavis Laboratories FL Inc. on December 16, 2016 in Weston, 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
December 16, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Weston, FL (United States)