FDA Inspection 701878 - iRhythm Technologies Inc - December 14, 2010

FDA Inspection 701878 for iRhythm Technologies Inc on December 14, 2010. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 701878 for iRhythm Technologies Inc on December 14, 2010. Classification: No Action Indicated (NAI).

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Record Information

Company

iRhythm Technologies Inc

Inspection Date

December 14, 2010

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 2524ab41-80fd-4d42-a426-820895f14a8b

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