FDA Inspection 1029822 - Haussen, Diogo - September 26, 2017

Record Details

This FDA Inspection record concerns Haussen, Diogo, with an inspection on September 26, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Haussen, Diogo
Inspection Date: September 26, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 20e0b00c-634c-4933-aeeb-ef58bf37d8d2