FDA Inspection 900803 - Kai Yi Co. - September 23, 2014

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Record Details

This FDA Inspection record concerns Kai Yi Co., with an inspection on September 23, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Kai Yi Co.
Inspection Date: September 23, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 80d90847-a176-489b-88cf-def7a63be113

Violation Codes1

21 CFR 820.198(a)

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