FDA inspection
Kedrion S.p.A.: FDA inspection ending Apr 18, 2012
FDA inspection 785499 · Voluntary Action Indicated (VAI) · Gallicano
Key facts
| Inspection ID | 785499 |
|---|---|
| Firm | Kedrion S.p.A. |
| FEI number | 3008919567 |
| Address | Via Di Fondovalle |
| City | Gallicano |
| Country | Italy |
| Fiscal year | 2012 |
| Inspection end date | Apr 18, 2012 |
| 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