# FDA Inspection 819842 - Askion Gmbh - January 31, 2013

Source: https://www.keypedia.com/records/fda_inspections/askion-gmbh/192f91b3-01b4-42d7-9d77-7c5dc5acedb2
Source feed: FDA_Inspections

> FDA Inspection 819842 for Askion Gmbh on January 31, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 819842
- Company Name: Askion Gmbh
- Inspection Date: 2013-01-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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