FDA Inspection 1000624 - L&K Biomed Co., Ltd. - January 26, 2017

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Record Details

This FDA Inspection record concerns L&K Biomed Co., Ltd., with an inspection on January 26, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: L&K Biomed Co., Ltd.
Inspection Date: January 26, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5f4faeb9-90bd-4080-a516-8b7c866afa54