FDA Inspection 820317 - iRhythm Technologies Inc - February 28, 2013

FDA Inspection 820317 for iRhythm Technologies Inc on February 28, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 820317 for iRhythm Technologies Inc on February 28, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

iRhythm Technologies Inc

Inspection Date

February 28, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 267055c8-6147-4058-8490-5375ec8ea11b

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