FDA inspection
SIT SORDINA IORT TECHNOLOGIES SPA: FDA inspection ending Apr 18, 2018
FDA inspection 1081486 · Voluntary Action Indicated (VAI) · Vicenza
Key facts
| Inspection ID | 1081486 |
|---|---|
| Firm | SIT SORDINA IORT TECHNOLOGIES SPA |
| FEI number | 3010625741 |
| Address | Galleria Del Pozzo Rosso 13 |
| City | Vicenza |
| Fiscal year | 2018 |
| Inspection end date | Apr 18, 2018 |
| 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