# Guangdong Baihe Medical Technology Co., Ltd, Foshan, China – FDA Inspections

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

> Inspection records and compliance data for Guangdong Baihe Medical Technology Co., Ltd in Foshan. 3 FDA inspections on record (1 OAI), 1 Form 483, 1 warning letter, last inspected August 24, 2017.

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## Details

- Name: Guangdong Baihe Medical Technology Co., Ltd
- FEI Number: 3006621386
- Address Line 1: Building 2, Building3-6f Building F 3-4, No. 89 Kezhi East Rd; Shishanzhen Nanhai
- City: Foshan
- Country Name: China
- Address: Building 2, Building3-6f Building F 3-4, No. 89 Kezhi East Rd; Shishanzhen Nanhai, Foshan, China
- Country: China

## Related Documents

- FDA Inspection 1027009 - Guangdong Baihe Medical Technology Co., Ltd - 2017-08-24 — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2017
- [FDA Inspection 1027009 - Guangdong Baihe Medical Technology Co., Ltd - 2017-08-24](https://www.keypedia.com/records/fda_inspections/guangdong-baihe-medical-technology-co-ltd/f3fb1325-9dd8-40d9-9026-c87d84106ae4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 24, 2017
- FDA Inspection 828938 - Guangdong Baihe Medical Technology Co., Ltd - 2013-03-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 21, 2013
- FDA Inspection 828938 - Guangdong Baihe Medical Technology Co., Ltd - 2013-03-21 — classification: No Action Indicated (NAI), source: FDA, date: March 21, 2013
- [WARNING_LETTER - Guangdong Baihe Medical Technology Co., Ltd - 2012-03-30](https://www.keypedia.com/records/warning_letter/guangdong-baihe-medical-technology-co-ltd/bb83eeab-4c7f-4e50-9cc8-9fe0720b784c) — source: FDA, date: March 30, 2012
- [FDA Inspection 775617 - Guangdong Baihe Medical Technology Co., Ltd - 2012-03-30](https://www.keypedia.com/records/fda_inspections/guangdong-baihe-medical-technology-co-ltd/cd639833-e931-47fe-aa1b-cf1821cb5dad) — classification: Official Action Indicated (OAI), source: FDA, date: March 30, 2012

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