FDA Inspection 1303528 — Takeda Manufacturing Austria AG

Takeda Manufacturing Austria AG — FEI 3003046565

The FDA completed an inspection of Takeda Manufacturing Austria AG on May 18, 2026 in Orth An Der Donau. 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
May 18, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Orth An Der Donau (Austria)