# Chongqing Kanghua Ruiming S&T Co., Ltd. – FDA Inspection, Sep 5, 2019

Source: https://www.keypedia.com/records/fda_inspections/chongqing-kanghua-ruiming-st-co-ltd/ff70e84c-ca59-488c-b070-90cfef556aa1
Source feed: FDA_Inspections

> FDA inspection 1107000 of Chongqing Kanghua Ruiming S&T Co., Ltd., September 05, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1107000
- Company Name: Chongqing Kanghua Ruiming S&T Co., Ltd.
- Inspection Date: 2019-09-05
- 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: 0

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/kelvin-cheung/ded61aee-4b4b-4049-a67c-19d971475be7)

Company: https://www.keypedia.com/companies/chongqing-kanghua-ruiming-st-co-ltd/b4400d95-a3b5-48e1-926d-ae4b5163442c

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