FDA Inspection 1002468 — Patheon Inc.

Patheon Inc. — FEI 3003516812

The FDA completed an inspection of Patheon Inc. on Dec 9, 2016 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
Dec 9, 2016
Fiscal Year
2017
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.