FDA Inspection 956228 - Tochigi Seiko Kk - December 17, 2015

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Record Details

This FDA Inspection record concerns Tochigi Seiko Kk, with an inspection on December 17, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Tochigi Seiko Kk
Inspection Date: December 17, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 87878381-7d93-4007-a46f-013e6a73c4c1