FDA inspection
Kedrion S.p.A.: FDA inspection ending Apr 10, 2025
FDA inspection 1281078 · No Action Indicated (NAI) · Gallicano
Key facts
| Inspection ID | 1281078 |
|---|---|
| Firm | Kedrion S.p.A. |
| FEI number | 3008919567 |
| Address | Via Di Fondovalle |
| City | Gallicano |
| Fiscal year | 2025 |
| Inspection end date | Apr 10, 2025 |
| 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
- 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