FDA Inspection 1210849 — Weidmann Medical Technology AG
The FDA completed an inspection of Weidmann Medical Technology AG on July 4, 2023 in Bad Ragaz. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 4, 2023
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bad Ragaz (Switzerland)