# FDA Inspection 774232 - Koko GmbH - February 23, 2012

Source: https://www.keypedia.com/records/fda_inspections/koko-gmbh/2b826630-907c-4c28-9caa-c3a21d069237
Source feed: FDA_Inspections

> FDA Inspection 774232 for Koko GmbH on February 23, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 774232
- Company Name: Koko GmbH
- Inspection Date: 2012-02-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 774232 - 2012-02-23](https://www.keypedia.com/records/fda_inspections/koko-gmbh/ebf3f1b5-63a8-4496-8668-769671f90cff)

Company: https://www.keypedia.com/companies/koko-gmbh/cdb1522f-58f4-4da0-8e16-aad4beb9a942

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