FDA Inspection 981370 - FIT-PRO KFT LTD - July 19, 2016

FDA Inspection 981370 for FIT-PRO KFT LTD on July 19, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 981370 for FIT-PRO KFT LTD on July 19, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

FIT-PRO KFT LTD

Inspection Date

July 19, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f6522de1-e62e-47c8-a6a5-d0ac9a3c633a

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