FDA Inspection 1025913 - Q-Med AB - August 24, 2017

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Record Details

This FDA Inspection record concerns Q-Med AB, with an inspection on August 24, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Q-Med AB
Inspection Date: August 24, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 40bd27d0-f201-48fa-ac1c-a1c38686bb0d