FDA Inspection 833835 - iRhythm Technologies, Inc. - May 24, 2013

FDA Inspection 833835 for iRhythm Technologies, Inc. on May 24, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 833835 for iRhythm Technologies, Inc. on May 24, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.184

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Record Information

Company

iRhythm Technologies, Inc.

Inspection Date

May 24, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ff2cdc6a-fc5a-4bfe-856f-e672c462eeb8

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