FDA Inspection
Palodex Group OyPalodex Group Oy – FDA Inspection, Sep 5, 2012
Record Details
This FDA Inspection record concerns Palodex Group Oy, with an inspection on September 5, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Palodex Group Oy
- Inspection Date
- September 5, 2012
- Product Type
- Devices
View Company Profile
ID · a63bb128-0bbf-4a49-b398-1a8b85458552
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 800785
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
Other FDA inspections of Palodex Group Oy
5| Date | Classification | Office | Project area |
|---|---|---|---|
| August 16, 2019 | Not classified | Office of Inspections and Investigations | |
| January 31, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 4, 2015 | 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 1082204 - 2019-01-31
- FDA Inspection 944319 - 2015-09-04
- FDA Inspection 669980 - 2009-09-30
- FDA Inspection 669974 - 2009-09-30
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