FDA Inspection 1038513 - Hiossen Inc. - April 24, 2017

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Record Details

This FDA Inspection record concerns Hiossen Inc., with an inspection on April 24, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Hiossen Inc.
Inspection Date: April 24, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6c2920e7-6c58-4424-9703-46b4cfcbb7a7