FDA Warning Letter — Actavis Elizabeth LLC

Case 83426 — FEI 2211563

The FDA took a Warning Letter action against Actavis Elizabeth LLC on Feb 18, 2010 (Elizabeth, NJ). 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 Elizabeth LLC
Date
Feb 18, 2010
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Elizabeth, NJ (United States)

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