# BAK KOHLER Medical KG – FDA Inspection, Jan 19, 2012

Source: https://www.keypedia.com/records/fda_inspections/bak-kohler-medical-kg/be8455d1-88bd-41fa-9a60-f9f6f6c96070
Source feed: FDA_Inspections

> FDA inspection 768246 of BAK KOHLER Medical KG, January 19, 2012. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 768246
- Company Name: BAK KOHLER Medical KG
- Inspection Date: 2012-01-19
- 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: 3

## Related Documents

- [FDA Inspection 1066877 - 2018-09-27](https://www.keypedia.com/records/fda_inspections/bak-kohler-medical-kg/b3b69890-7f75-4d80-a017-deba07538397)

Company: https://www.keypedia.com/companies/bak-kohler-medical-kg/b0b8684e-ecda-4a01-83bb-8a43049dad9b

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