# FDA Inspection 1210849 - Weidmann Medical Technology AG - July 04, 2023

Source: https://www.keypedia.com/records/fda_inspections/weidmann-medical-technology-ag/adfb1121-d127-4300-8bfc-c4fad5b61dc0
Source feed: FDA_Inspections

> FDA Inspection 1210849 for Weidmann Medical Technology AG on July 04, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1210849
- Company Name: Weidmann Medical Technology AG
- Inspection Date: 2023-07-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/weidmann-medical-technology-ag/93db5ea1-ebff-4a52-9c0a-f571c5b9c7cd

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7