FDA Inspection
Palodex Group OyPalodex Group Oy – FDA Inspection, Aug 16, 2019
Record Details
This FDA Inspection record concerns Palodex Group Oy, with an inspection on August 16, 2019, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Palodex Group Oy
- Inspection Date
- August 16, 2019
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · b5fe5add-796e-4ebe-9965-eb49504f276b
Inspection Facts
- Inspection number
- 1156767
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Palodex Group Oy
5| Date | Classification | Office | Project area |
|---|---|---|---|
| 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 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 1082204 - 2019-01-31
- 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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