FDA inspection
EUROSIREL S.P.A: FDA inspection ending May 24, 2024
FDA inspection 1243970 · Official Action Indicated (OAI) · Cusago
Key facts
| Inspection ID | 1243970 |
|---|---|
| Firm | EUROSIREL S.P.A |
| FEI number | 3015892095 |
| Address | Viale Europa 30 |
| City | Cusago |
| Country | Italy |
| Fiscal year | 2024 |
| Inspection end date | May 24, 2024 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
| Warning letter | 690733 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes 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