FDA Inspection 683389 — Apotex Inc.

Apotex Inc. — FEI 3001617666

The FDA completed an inspection of Apotex Inc. on Aug 17, 2010 in Richmond Hill. 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
Aug 17, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Richmond Hill (Canada)

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