FDA Inspection 1078546 — Takeda Austria GmbH

Takeda Austria GmbH — FEI 3001157285

The FDA completed an inspection of Takeda Austria GmbH on November 9, 2018 in Linz. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 9, 2018
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Linz (Austria)