FDA Inspection 734601 — Patheon Inc.

Patheon Inc. — FEI 3003516812

The FDA completed an inspection of Patheon Inc. on Jul 7, 2011 in Whitby. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jul 7, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Whitby (Canada)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.