FDA Inspection
Askion GmbhAskion Gmbh – FDA Inspection, Jan 17, 2020
Record Details
This FDA Inspection record concerns Askion Gmbh, with an inspection on January 17, 2020, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Askion Gmbh
- Inspection Date
- January 17, 2020
- Product Type
- Devices
View Company Profile
ID · f5a0ffb5-829e-4d7c-ac4e-5d7852de0e2a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1116092
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 820.100(b)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Askion Gmbh
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 20, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 31, 2013 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 3, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Askion Gmbh
- FDA Inspection 948857 - 2015-11-20
- FDA Inspection 819842 - 2013-01-31
- FDA Inspection 623328 - 2009-09-03
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.