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: de6bb60d-130b-403e-907c-7a23f920ce58

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