FDA inspection
Technomed Europe: FDA inspection ending Apr 21, 2016
FDA inspection 969980 · No Action Indicated (NAI) · Maastricht-Airport
Key facts
| Inspection ID | 969980 |
|---|---|
| Firm | Technomed Europe |
| FEI number | 3001450493 |
| Address | Amerikalaan 71 |
| City | Maastricht-Airport |
| Country | Netherlands |
| Fiscal year | 2016 |
| Inspection end date | Apr 21, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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