FDA inspection
Ermis MedTech GmbH: FDA inspection ending Aug 29, 2019
FDA inspection 1102918 · No Action Indicated (NAI) · Tuttlingen
Key facts
| Inspection ID | 1102918 |
|---|---|
| Firm | Ermis MedTech GmbH |
| FEI number | 3005071827 |
| Address | Dornierstr. 49 |
| City | Tuttlingen |
| Country | Germany |
| Fiscal year | 2019 |
| Inspection end date | Aug 29, 2019 |
| 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