# FDA Inspection 1027009 - Guangdong Baihe Medical Technology Co., Ltd - August 24, 2017

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

> FDA Inspection 1027009 for Guangdong Baihe Medical Technology Co., Ltd on August 24, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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