FDA Inspection 976467 - iRhythm Technologies Inc - June 29, 2016

FDA Inspection 976467 for iRhythm Technologies Inc on June 29, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 976467 for iRhythm Technologies Inc on June 29, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

iRhythm Technologies Inc

Inspection Date

June 29, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: a63ddfa0-57ad-4e50-9853-4cc1fb324511

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