FDA Inspection 1008837 - MAI/GENESIS - April 05, 2017

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Record Details

This FDA Inspection record concerns MAI/GENESIS, with an inspection on April 5, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: MAI/GENESIS
Inspection Date: April 5, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b086d801-589a-41cf-aa19-029297da6ed6