FDA Inspection 1331016 — Takeda Manufacturing Austria AG

Takeda Manufacturing Austria AG — FEI 3002807133

The FDA completed an inspection of Takeda Manufacturing Austria AG on Jul 17, 2026 in Vienna. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 17, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Vienna (Austria)