# Guangdong Baihe Medical Technology Co., Ltd – FDA Inspection, Aug 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/guangdong-baihe-medical-technology-co-ltd/f3fb1325-9dd8-40d9-9026-c87d84106ae4
Source feed: FDA_Inspections

> FDA inspection 1027009 of Guangdong Baihe Medical Technology Co., Ltd, August 24, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1027009
- Company Name: Guangdong Baihe Medical Technology Co., Ltd
- Inspection Date: 2017-08-24
- 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: 0

## Related Documents

- FDA Inspection 828938 - 2013-03-21
- [FDA Inspection 775617 - 2012-03-30](https://www.keypedia.com/records/fda_inspections/guangdong-baihe-medical-technology-co-ltd/cd639833-e931-47fe-aa1b-cf1821cb5dad)

## Related Officers

- [Dianiris C. Ayala](https://www.keypedia.com/people/dianiris-c-ayala/ba6c5538-201b-4c9a-8f23-e160db6868e6)

Company: https://www.keypedia.com/companies/guangdong-baihe-medical-technology-co-ltd/79d2e901-9843-48f0-8311-ef9f3c32b884

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