FDA Inspection 984850 - Kaylight Corporation - September 12, 2016

FDA Inspection 984850 for Kaylight Corporation on September 12, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 984850 for Kaylight Corporation on September 12, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Kaylight Corporation

Inspection Date

September 12, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa995cd6-9cb0-4b35-9a3e-2d309af1bf67

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