FDA Inspection
Q-Med ABFDA Inspection 789285 - Q-Med AB - June 21, 2012
Record Details
This FDA Inspection record concerns Q-Med AB, with an inspection on June 21, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Q-Med AB
- Inspection Date
- June 21, 2012
- Product Type
- Devices
View Company Profile
ID · fb513c8e-77af-4151-9a93-b3c6599e7159
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 789285
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
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 |
| August 24, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 13, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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 1025913 - 2017-08-24
- FDA Inspection 921654 - 2015-02-13
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