IDT Electronics (Shenzhen) Co., Ltd. – FDA Inspection, Jun 1, 2017

Record Details

This FDA Inspection record concerns IDT Electronics (Shenzhen) Co., Ltd., with an inspection on June 1, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: IDT Electronics (Shenzhen) Co., Ltd.
Inspection Date: June 1, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Ashley A. Mutawakkil (Investigator)

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ID · e352d559-df80-4435-bfe7-58c96fcfee8a

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number: 1016239
FDA center: Medical Devices & Rad Health
Project area: Postmarket Assurance: Devices
Outcome: Form 483 issued

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FDA Inspection

IDT Electronics (Shenzhen) Co., Ltd.June 1, 2017