# FDA Inspection 1198120 - Bernd Richter GmbH - February 16, 2023

Source: https://www.keypedia.com/records/fda_inspections/bernd-richter-gmbh/09e32135-f49b-486b-b70b-a82427fb252c
Source feed: FDA_Inspections

> FDA Inspection 1198120 for Bernd Richter GmbH on February 16, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1198120
- Company Name: Bernd Richter GmbH
- Inspection Date: 2023-02-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/bernd-richter-gmbh/412d5fc6-4581-420a-9bd5-3f99b9a8e273

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