FDA Inspection 1001291 - Mighty Oak Medical - January 13, 2017

FDA Inspection 1001291 for Mighty Oak Medical on January 13, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1001291 for Mighty Oak Medical on January 13, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Mighty Oak Medical

Inspection Date

January 13, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb4359b5-2091-4728-9a92-6e6ea1fa7076

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