FDA Inspection 1040786 - Nihon Kohden America LLC - October 26, 2017

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Record Details

This FDA Inspection record concerns Nihon Kohden America LLC, with an inspection on October 26, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Nihon Kohden America LLC
Inspection Date: October 26, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ec0effbe-7583-4a4f-96d8-246783364bbd