FDA Inspection 610738 — Apotex Inc.

Apotex Inc. — FEI 3002906944

The FDA completed an inspection of Apotex Inc. on August 14, 2009 in North York. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 14, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
North York (Canada)