FDA Inspection 988533 - Caremaster Technology (Hk) Group Co., Ltd - September 22, 2016

FDA Inspection 988533 for Caremaster Technology (Hk) Group Co., Ltd on September 22, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 988533 for Caremaster Technology (Hk) Group Co., Ltd on September 22, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Caremaster Technology (Hk) Group Co., Ltd

Inspection Date

September 22, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fbe340b6-b8a6-4d5d-8f7e-106721518be2

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