# Shenzhen Zifound Infonet Technology Co., Ltd. – FDA Inspection, Jan 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-zifound-infonet-technology-co-ltd/b26bf43c-91ad-4b23-80da-45e4d04e4148
Source feed: FDA_Inspections

> FDA inspection 1003123 of Shenzhen Zifound Infonet Technology Co., Ltd., January 26, 2017. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003123
- Company Name: Shenzhen Zifound Infonet Technology Co., Ltd.
- Inspection Date: 2017-01-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- [FDA Inspection 1063881 - 2018-07-19](https://www.keypedia.com/records/fda_inspections/shenzhen-zifound-infonet-technology-co-ltd/b082755e-da28-486a-90c9-0c88f7a30a01)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/andrea-a-branche/9ffe9b53-7963-49a6-be4e-25e644f1759f)

Company: https://www.keypedia.com/companies/shenzhen-zifound-infonet-technology-co-ltd/0ef3d7dd-9804-4702-8c4b-a6355616e59f

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