FDA Inspection 712527 — Apotex Inc.

Apotex Inc. — FEI 3002906944

The FDA completed an inspection of Apotex Inc. on Feb 11, 2011 in North York. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 11, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
North York (Canada)

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