FDA Inspection 838849 - Lutonix Inc. - June 25, 2013

FDA Inspection 838849 for Lutonix Inc. on June 25, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 838849 for Lutonix Inc. on June 25, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

Lutonix Inc.

Inspection Date

June 25, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 5f719fdd-d11a-4914-90aa-6bef8a51919f

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