FDA inspection
Weidmann Medical Technology AG: FDA inspection ending Jul 4, 2023
FDA inspection 1210849 · No Action Indicated (NAI) · Bad Ragaz
Key facts
| Inspection ID | 1210849 |
|---|---|
| Firm | Weidmann Medical Technology AG |
| FEI number | 3003041175 |
| Address | Industriestrasse 96 |
| City | Bad Ragaz |
| Country | Switzerland |
| Fiscal year | 2023 |
| Inspection end date | Jul 4, 2023 |
| 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