FDA Inspection 976246 — Patheon Inc.

Patheon Inc. — FEI 3003516812

The FDA completed an inspection of Patheon Inc. on February 26, 2016 in Whitby. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 26, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Whitby (Canada)