FDA Inspection
Guangdong Baihe Medical Technology Co., LtdGuangdong Baihe Medical Technology Co., Ltd – FDA Inspection, Aug 24, 2017
Record Details
This FDA Inspection record concerns Guangdong Baihe Medical Technology Co., Ltd, with an inspection on August 24, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · f3fb1325-9dd8-40d9-9026-c87d84106ae4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1027009
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Guangdong Baihe Medical Technology Co., Ltd
2| Date | Classification | Office | Project area |
|---|---|---|---|
| March 21, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 30, 2012 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Guangdong Baihe Medical Technology Co., Ltd
- FDA Inspection 828938 - 2013-03-21
- FDA Inspection 775617 - 2012-03-30
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