FDA Inspection 1279403 — Actavis Laboratories FL Inc.

Actavis Laboratories FL Inc. — FEI 3003937607

The FDA completed an inspection of Actavis Laboratories FL Inc. on Jul 18, 2025 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
Jul 18, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Weston, FL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.