FDA inspection
Euromi S.A.: FDA inspection ending Jan 15, 2015
FDA inspection 914498 · Official Action Indicated (OAI) · Dison
Key facts
| Inspection ID | 914498 |
|---|---|
| Firm | Euromi S.A. |
| FEI number | 3007697975 |
| Address | Z. I. de Lambermont, Rue des Ormes 151 |
| City | Dison |
| Country | Belgium |
| Fiscal year | 2015 |
| Inspection end date | Jan 15, 2015 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 456931 |
At a glance
- 10–99 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