# FDA Inspection 1228844 - Bauerfeind AG - February 08, 2024

Source: https://www.keypedia.com/records/fda_inspections/bauerfeind-ag/77feb47f-a826-45be-8ca4-ab71a37ffc85
Source feed: FDA_Inspections

> FDA Inspection 1228844 for Bauerfeind AG on February 08, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1228844
- Company Name: Bauerfeind AG
- Inspection Date: 2024-02-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1228844 - 2024-02-08](https://www.keypedia.com/records/fda_inspections/bauerfeind-ag/7668cb72-2973-4ae7-af46-041840a454a2)
- [FDA Inspection 993016 - 2016-11-04](https://www.keypedia.com/records/fda_inspections/bauerfeind-ag/f9b5a6cf-b414-42e1-9534-9699e6d8057c)
- [FDA Inspection 993016 - 2016-11-04](https://www.keypedia.com/records/fda_inspections/bauerfeind-ag/039cffd5-d1ae-4c73-9a43-651993d7613e)

Company: https://www.keypedia.com/companies/bauerfeind-ag/bbfdc230-c7c2-41f7-a32b-43eed35a2604

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