FDA Inspection 1279948 — Takeda Austria GmbH

Takeda Austria GmbH — FEI 3001157285

The FDA completed an inspection of Takeda Austria GmbH on February 14, 2025 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 14, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Linz (Austria)

Additional Details

Mutual Recognition Agreement (MRA)