FDA Inspection 568263 — Patheon Inc.

Patheon Inc. — FEI 3003516812

The FDA completed an inspection of Patheon Inc. on Jan 27, 2009 in Whitby. 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
Jan 27, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Whitby (Canada)

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