FDA Inspection 963674 — Takeda Manufacturing Austria AG
The FDA completed an inspection of Takeda Manufacturing Austria AG on Mar 1, 2016 in Orth An Der Donau. 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: Biologics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Mar 1, 2016
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Orth An Der Donau (Austria)