FDA inspection
Takeda Manufacturing Austria AG: FDA inspection ending May 18, 2026
FDA inspection 1303528 · No Action Indicated (NAI) · Orth An Der Donau
Key facts
| Inspection ID | 1303528 |
|---|---|
| Firm | Takeda Manufacturing Austria AG |
| FEI number | 3003046565 |
| Address | Uferstrase 15 |
| City | Orth An Der Donau |
| Country | Austria |
| Fiscal year | 2026 |
| Inspection end date | May 18, 2026 |
| Classification | No Action Indicated (NAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data