# Guangdong Baihe Medical Technology Co., Ltd – FDA Inspection, Mar 30, 2012

Source: https://www.keypedia.com/records/fda_inspections/guangdong-baihe-medical-technology-co-ltd/cd639833-e931-47fe-aa1b-cf1821cb5dad
Source feed: FDA_Inspections

> FDA inspection 775617 of Guangdong Baihe Medical Technology Co., Ltd, March 30, 2012. Classification: Official Action Indicated (OAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 775617
- Company Name: Guangdong Baihe Medical Technology Co., Ltd
- Inspection Date: 2012-03-30
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- 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 1027009 - 2017-08-24](https://www.keypedia.com/records/fda_inspections/guangdong-baihe-medical-technology-co-ltd/f3fb1325-9dd8-40d9-9026-c87d84106ae4)
- FDA Inspection 828938 - 2013-03-21

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