# Askion Gmbh – FDA Inspection, Jan 17, 2020

Source: https://www.keypedia.com/records/fda_inspections/askion-gmbh/f5a0ffb5-829e-4d7c-ac4e-5d7852de0e2a
Source feed: FDA_Inspections

> FDA inspection 1116092 of Askion Gmbh, January 17, 2020. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1116092
- Company Name: Askion Gmbh
- Inspection Date: 2020-01-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 948857 - 2015-11-20
- FDA Inspection 819842 - 2013-01-31
- FDA Inspection 623328 - 2009-09-03

Company: https://www.keypedia.com/companies/askion-gmbh/e793e415-7271-4fd9-bc67-04f37cf8916c

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