FDA Inspection 932720 — Patheon Austria GmbH & Co. KG

Patheon Austria GmbH & Co. KG — FEI 3002806853

The FDA completed an inspection of Patheon Austria GmbH & Co. KG on May 29, 2015 in Linz. 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
May 29, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Linz (Austria)