FDA inspection
Takeda Manufacturing Italia SPA: FDA inspection ending Nov 15, 2019
FDA inspection 1114886 · Voluntary Action Indicated (VAI) · Cittaducale
Key facts
| Inspection ID | 1114886 |
|---|---|
| Firm | Takeda Manufacturing Italia SPA |
| FEI number | 3007244131 |
| Address | S. Rufina, Cittaducale, Via della Chimica 5 |
| City | Cittaducale |
| Country | Italy |
| Fiscal year | 2020 |
| Inspection end date | Nov 15, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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