# iRhythm Technologies Inc - Inspection Records

Source: https://www.keypedia.com/companies/irhythm-technologies-inc/fb230c01-1845-46a2-82fa-5eda280fcc0c

> Inspection records and compliance data for iRhythm Technologies Inc in San Francisco, California. Access full analysis and detailed observations.

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## Details

- Name: iRhythm Technologies Inc
- FEI Number: 3007208829
- City: San Francisco
- State: California
- Country Name: United States
- Address Line 1: 699 8th St Ste 600
- Zip Code: 94103

## Related Documents

- [483 - iRhythm Technologies Inc - 2024-07-31](https://www.keypedia.com/records/483/irhythm-technologies-inc/e564eb67-aace-4b72-a666-d2a4e1c4a692) — source: FDA, date: July 31, 2024
- [483 - iRhythm Technologies Inc - 2024-07-31](https://www.keypedia.com/records/483/irhythm-technologies-inc/ad37cc26-32dc-4534-86e3-30dc55f7191d) — source: FDA, date: July 31, 2024
- [483 - iRhythm Technologies Inc - 2024-07-31](https://www.keypedia.com/records/483/irhythm-technologies-inc/b1bd87c7-6730-4818-9dce-829d61d2f320) — source: FDA, date: July 31, 2024
- [FDA Inspection 1245190 - iRhythm Technologies Inc - 2024-07-31](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/bee72d5f-6c26-4e0f-b651-273d18bd14ff) — classification: Official Action Indicated (OAI), source: FDA, date: July 31, 2024
- [FDA Inspection 1245190 - iRhythm Technologies Inc - 2024-07-31](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/6a2a632d-b06e-4297-b445-739e2e30fa2f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 31, 2024
- [FDA Inspection 976467 - iRhythm Technologies Inc - 2016-06-29](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/a63ddfa0-57ad-4e50-9853-4cc1fb324511) — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2016
- [FDA Inspection 976467 - iRhythm Technologies Inc - 2016-06-29](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/de6bb60d-130b-403e-907c-7a23f920ce58) — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2016
- [FDA Inspection 820317 - iRhythm Technologies Inc - 2013-02-28](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/267055c8-6147-4058-8490-5375ec8ea11b) — classification: No Action Indicated (NAI), source: FDA, date: February 28, 2013
- [FDA Inspection 701878 - iRhythm Technologies Inc - 2010-12-14](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/f0fd0e93-3252-4aaf-8f23-6317d6a85b3c) — classification: No Action Indicated (NAI), source: FDA, date: December 14, 2010
- [FDA Inspection 701878 - iRhythm Technologies Inc - 2010-12-14](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/2524ab41-80fd-4d42-a426-820895f14a8b) — classification: No Action Indicated (NAI), source: FDA, date: December 14, 2010

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