# Palodex Group Oy – FDA Inspection, Sep 5, 2012

Source: https://www.keypedia.com/records/fda_inspections/palodex-group-oy/a63bb128-0bbf-4a49-b398-1a8b85458552
Source feed: FDA_Inspections

> FDA inspection 800785 of Palodex Group Oy, September 05, 2012. Classification: Voluntary Action Indicated (VAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 800785
- Company Name: Palodex Group Oy
- Inspection Date: 2012-09-05
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

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- [FDA Inspection 1082204 - 2019-01-31](https://www.keypedia.com/records/fda_inspections/palodex-group-oy/fe34267f-d24f-4d26-b840-e7105043fb27)
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Company: https://www.keypedia.com/companies/palodex-group-oy/a133e74f-4bd4-48d4-b630-978673ba524b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
