Shenzhen OKFAN Electronics Co., Ltd. – FDA Inspection, Dec 8, 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
Person: Andre S. Lamontagne (Issuing Officer)

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

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number: 1060869
FDA center: Medical Devices & Rad Health
Project area: Radiation Control and Health Safety Act

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FDA Inspection

Shenzhen OKFAN Electronics Co., Ltd.December 8, 2017