# ASSKEA GmbH – FDA Inspection, Nov 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/asskea-gmbh/4bf6c6f5-14f5-44a2-8c16-5a90c04f69c4
Source feed: FDA_Inspections

> FDA inspection 1032109 of ASSKEA GmbH, November 17, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1032109
- Company Name: ASSKEA GmbH
- Inspection Date: 2017-11-17
- 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: 2

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

Company: https://www.keypedia.com/companies/asskea-gmbh/728e51b2-d1c2-47eb-9f19-63dedb463c81

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