# FDA Inspection 1077749 - iRhythm Technologies, Inc. - October 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/5a520e5d-e6e4-4abe-a6f3-59250e676dab
Source feed: FDA_Inspections

> FDA Inspection 1077749 for iRhythm Technologies, Inc. on October 30, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1077749
- Company Name: iRhythm Technologies, Inc.
- Inspection Date: 2018-10-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/irhythm-technologies-inc/22726654-c3a7-4b3b-9cc8-9d0032796ab3

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7