FDA Inspection 1014338 - Lutonix Inc. - May 24, 2017

FDA Inspection 1014338 for Lutonix Inc. on May 24, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1014338 for Lutonix Inc. on May 24, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Lutonix Inc.

Inspection Date

May 24, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 6c5868cf-b556-49e5-a560-2426d3cc3162

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