FDA Inspection 1077902 — Actavis Laboratories FL Inc.

Actavis Laboratories FL Inc. — FEI 3003937607

The FDA completed an inspection of Actavis Laboratories FL Inc. on Jan 23, 2019 in Weston, FL. 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
Jan 23, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Weston, FL (United States)

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