FDA Inspection 828938 - Guangdong Baihe Medical Technology Co., Ltd - March 21, 2013

FDA Inspection 828938 for Guangdong Baihe Medical Technology Co., Ltd on March 21, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 828938 for Guangdong Baihe Medical Technology Co., Ltd on March 21, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Guangdong Baihe Medical Technology Co., Ltd

Inspection Date

March 21, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 6e0ad8f3-d5d9-47f9-a45b-d5f67de40559

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