FDA Inspection 762022 - Nihon Kohden Tomioka Corporation - December 09, 2011

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Record Details

This FDA Inspection record concerns Nihon Kohden Tomioka Corporation, with an inspection on December 9, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company: Nihon Kohden Tomioka Corporation
Inspection Date: December 9, 2011
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4f22c994-d1c9-49c7-b413-96fbb551d08a