# FDA Inspection 1116092 - Askion Gmbh - January 17, 2020

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

> FDA Inspection 1116092 for Askion Gmbh on January 17, 2020. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1116092 - 2020-01-17](https://www.keypedia.com/records/fda_inspections/askion-gmbh/7584de0a-060f-4864-878d-872d0a377ed3)
- [FDA Inspection 1116092 - 2020-01-17](https://www.keypedia.com/records/fda_inspections/askion-gmbh/3001d3e2-7511-4072-b952-b9d98329050b)
- [FDA Inspection 948857 - 2015-11-20](https://www.keypedia.com/records/fda_inspections/askion-gmbh/6a3a2c66-e2ed-4c2a-8186-a0d224ebc25b)
- [FDA Inspection 948857 - 2015-11-20](https://www.keypedia.com/records/fda_inspections/askion-gmbh/2208527e-545c-4fd3-bbb1-b19b428bcf2c)
- [FDA Inspection 819842 - 2013-01-31](https://www.keypedia.com/records/fda_inspections/askion-gmbh/65d7912a-6af2-4505-ad25-5a2a9e51637d)

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