FDA Inspection 966635 - Indulis Kumsars, MD - March 10, 2016

FDA Inspection 966635 for Indulis Kumsars, MD on March 10, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 966635 for Indulis Kumsars, MD on March 10, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Indulis Kumsars, MD

Inspection Date

March 10, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f93593ec-7fce-4c76-a485-79dfe1eafec5

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