FDA Inspection 1000388 - Medos S.A. - December 08, 2016

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Record Details

This FDA Inspection record concerns Medos S.A., with an inspection on December 8, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medos S.A.
Inspection Date: December 8, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1bef30f7-2322-4bd3-aa53-f8d774dc5745