FDA Inspection
Q-Med ABQ-Med AB – FDA Inspection, Aug 24, 2017
Record Details
This FDA Inspection record concerns Q-Med AB, with an inspection on August 24, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · ebec262d-2d9e-4346-9d98-31e8bf2afa18
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1025913
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Q-Med AB
7| Date | Classification | Office | Project area |
|---|---|---|---|
| March 27, 2026 | Not classified | Office of Inspections and Investigations | |
| January 19, 2023 | NAI | Bioresearch Monitoring | |
| March 29, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 13, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 21, 2012 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Q-Med AB
- FDA Inspection 1313816 - 2026-03-27
- FDA Inspection 1199979 - 2023-01-19
- FDA Inspection 1048550 - 2018-03-29
- FDA Inspection 921654 - 2015-02-13
- FDA Inspection 789285 - 2012-06-21
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