FDA Inspection
Palodex Group OyPalodex Group Oy – FDA Inspection, Jan 31, 2019
Record Details
This FDA Inspection record concerns Palodex Group Oy, with an inspection on January 31, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · fe34267f-d24f-4d26-b840-e7105043fb27
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1082204
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Palodex Group Oy
5| Date | Classification | Office | Project area |
|---|---|---|---|
| August 16, 2019 | Not classified | Office of Inspections and Investigations | |
| September 4, 2015 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| September 5, 2012 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| September 30, 2009 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| September 30, 2009 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Palodex Group Oy
- FDA Inspection 1156767 - 2019-08-16
- FDA Inspection 944319 - 2015-09-04
- FDA Inspection 800785 - 2012-09-05
- FDA Inspection 669980 - 2009-09-30
- FDA Inspection 669974 - 2009-09-30
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