FDA inspection
EUROMI S.A.: FDA inspection ending Mar 2, 2023
FDA inspection 1198642 · Dison
Key facts
| Inspection ID | 1198642 |
|---|---|
| Firm | EUROMI S.A. |
| FEI number | 3007697975 |
| Address | Zi Des Plenesses, Rue Des Nouvelles Technologies 11 |
| City | Dison |
| Fiscal year | 2023 |
| Inspection end date | Mar 2, 2023 |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- 1–9 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