FDA Warning Letter — Actavis Laboratories FL, Inc.

Case 567857 — FEI 3003194604

The FDA took a Warning Letter action against Actavis Laboratories FL, Inc. on Feb 1, 2019 (Davie, FL). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Actavis Laboratories FL, Inc.
Date
Feb 1, 2019
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
Davie, FL (United States)

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