FDA Inspection 1029220 - Diatron US Inc. - September 06, 2017

Record Details

This FDA Inspection record concerns Diatron US Inc., with an inspection on September 6, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Diatron US Inc.
Inspection Date: September 6, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 9bbabf7c-1ad4-4c7b-bdf2-93368a89a6ad