FDA Inspection 996475 — Actavis Laboratories FL Inc.

Actavis Laboratories FL Inc. — FEI 3003937607

The FDA completed an inspection of Actavis Laboratories FL Inc. on Dec 16, 2016 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
Dec 16, 2016
Fiscal Year
2017
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.