FDA Inspection 794147 — Patheon Austria GmbH & Co. KG

Patheon Austria GmbH & Co. KG — FEI 3002806853

The FDA completed an inspection of Patheon Austria GmbH & Co. KG on Jun 1, 2012 in Linz. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 1, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Linz (Austria)