# Volker GmBH – FDA Inspection, Feb 26, 2015

Source: https://www.keypedia.com/records/fda_inspections/volker-gmbh/bfe9bdc0-9bd9-48dd-8428-04e16bd68aff
Source feed: FDA_Inspections

> FDA inspection 918030 of Volker GmBH, February 26, 2015. 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: 918030
- Company Name: Volker GmBH
- Inspection Date: 2015-02-26
- 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 803968 - 2012-09-27

Company: https://www.keypedia.com/companies/volker-gmbh/a65f546b-e4f3-4781-b2e3-b760e84682ee

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