BEIJING HONKON TECHNOLOGIES CO., LTD. – FDA Inspection, Sep 1, 2016

Record Details

This FDA Inspection record concerns BEIJING HONKON TECHNOLOGIES CO., LTD., with an inspection on September 1, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: BEIJING HONKON TECHNOLOGIES CO., LTD.
Inspection Date: September 1, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 697d2039-716d-4ab9-8eaf-f1c83eb5391b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number: 988018
FDA center: Medical Devices & Rad Health
Project area: Compliance: Devices

FDA Citations

21 CFR 820.30(g)Design validation - documentation

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FDA Inspection

BEIJING HONKON TECHNOLOGIES CO., LTD.September 1, 2016