# Weidmann Medical Technology AG – FDA Inspection, Jul 4, 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 of Weidmann Medical Technology AG, 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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/benjamin-w-anderson/a3c0961c-6a83-4bd7-abb8-02c5c8dd3a35)

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