FDA Inspection 660142 — Patheon Pharmaceuticals

Patheon Pharmaceuticals — FEI 3007154864

The FDA completed an inspection of Patheon Pharmaceuticals on Mar 24, 2010 in Blue Ash, OH. 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
Mar 24, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Blue Ash, OH (United States)

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