FDA Inspection 1082204 - Palodex Group Oy - January 31, 2019

FDA Inspection 1082204 for Palodex Group Oy on January 31, 2019. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1082204 for Palodex Group Oy on January 31, 2019. Classification: No Action Indicated (NAI).

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Record Information

Company

Palodex Group Oy

Inspection Date

January 31, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe34267f-d24f-4d26-b840-e7105043fb27

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