FDA Warning Letter — Apotex, Inc.

Case 58142 — FEI 3002808376

The FDA took a Warning Letter action against Apotex, Inc. on Jun 25, 2009 (Etobicoke, Canada). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Apotex, Inc.
Date
Jun 25, 2009
Fiscal Year
2009
Product Type
Drugs
Center
CDER
Location
Etobicoke (Canada)

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