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

FDA Inspection 1027009 for Guangdong Baihe Medical Technology Co., Ltd on August 24, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1027009 for Guangdong Baihe Medical Technology Co., Ltd on August 24, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Guangdong Baihe Medical Technology Co., Ltd

Inspection Date

August 24, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 32a8dcb7-4c99-48fb-aadc-bb23ed9562ac

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