FDA Inspection 1031382 - Simex Medizintechnik Gmbh - November 15, 2017

Record Details

This FDA Inspection record concerns Simex Medizintechnik Gmbh, with an inspection on November 15, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Simex Medizintechnik Gmbh
Inspection Date: November 15, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b4477be9-9d78-40c9-89d2-8725d79ef6d3