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

Source: https://www.keypedia.com/records/fda_inspections/beijing-honkon-technologies-co-ltd/697d2039-716d-4ab9-8eaf-f1c83eb5391b
Source feed: FDA_Inspections

> FDA inspection 988018 of BEIJING HONKON TECHNOLOGIES CO., LTD., September 01, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988018
- Company Name: BEIJING HONKON TECHNOLOGIES CO., LTD.
- Inspection Date: 2016-09-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

Company: https://www.keypedia.com/companies/beijing-honkon-technologies-co-ltd/6061121e-8bd0-4edb-a2b2-e6993e7d3470

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7