# FDA Inspection 803968 - Volker GmBH - September 27, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/volker-gmbh/dede49f7-d02a-4e5c-8a4c-0f80df7b18fb
Source feed: FDA_Inspections

> FDA Inspection 803968 for Volker GmBH on September 27, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803968
- Company Name: Volker GmBH
- Inspection Date: 2012-09-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 918030 - 2015-02-26](https://www.globalkeysolutions.net/records/fda_inspections/volker-gmbh/bfe9bdc0-9bd9-48dd-8428-04e16bd68aff)

Company: https://www.globalkeysolutions.net/companies/volker-gmbh/a65f546b-e4f3-4781-b2e3-b760e84682ee

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