FDA Inspection 1287706 — Actavis Laboratories FL, Inc.

Actavis Laboratories FL, Inc. — FEI 3003194604

The FDA completed an inspection of Actavis Laboratories FL, Inc. on November 18, 2025 in Davie, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 18, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Davie, FL (United States)

Citations

IDCFRDescription
103321 CFR 211.22(a)Authority lacking to review records, investigate errors
121321 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
201221 CFR 211.188(b)Batch production and Batch Control Record Requirements
202721 CFR 211.192Investigations of discrepancies, failures