FDA inspection
Eurospital S.P.A.: FDA inspection ending Jul 7, 2017
FDA inspection 1028360 · Voluntary Action Indicated (VAI) · Trieste
Key facts
| Inspection ID | 1028360 |
|---|---|
| Firm | Eurospital S.P.A. |
| FEI number | 1000553563 |
| Address | Via Flavia 122 |
| City | Trieste |
| Fiscal year | 2017 |
| Inspection end date | Jul 7, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
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