# Bernd Richter GmbH – FDA Inspection, Feb 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 of Bernd Richter GmbH, February 16, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1017385 - 2017-06-29](https://www.keypedia.com/records/fda_inspections/bernd-richter-gmbh/c04b584b-4bbd-4835-9cae-72e111c7ce4f)

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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