FDA Inspection 1060869 - Shenzhen OKFAN Electronics Co., Ltd. - December 08, 2017

Record Details

This FDA Inspection record concerns Shenzhen OKFAN Electronics Co., Ltd., with an inspection on December 8, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Shenzhen OKFAN Electronics Co., Ltd.
Inspection Date: December 8, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4b90884b-e629-4776-b9af-9120b7e139ee