FDA Inspection 1029050 - FootMaxx Inc. - September 19, 2017

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Record Details

This FDA Inspection record concerns FootMaxx Inc., with an inspection on September 19, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: FootMaxx Inc.
Inspection Date: September 19, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 49974e92-edfe-4a6d-b72e-5a0188df7e9c