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FDA Inspection 926808 — Takeda Austria GmbH

Takeda Austria GmbH — FEI 3001157285

The FDA completed an inspection of Takeda Austria GmbH on May 28, 2015 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
May 28, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Linz (Austria)

Facility

Other inspections at this facility

  • 1291316 (NAI Thu Sep 11 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1279948 (VAI Fri Feb 14 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1078546 (VAI Fri Nov 09 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1002607 (VAI Mon Jan 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 646574 (VAI Thu Feb 11 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources