FDA Inspection 953355 - Lutonix Inc. - December 17, 2015

FDA Inspection 953355 for Lutonix Inc. on December 17, 2015. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 953355 for Lutonix Inc. on December 17, 2015. Classification: No Action Indicated (NAI).

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Record Information

Company

Lutonix Inc.

Inspection Date

December 17, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 4106547e-7de3-446b-8ba8-5efd82ce520d

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