# iRhythm Technologies, Inc. - Inspection Records

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

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

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## Details

- Name: iRhythm Technologies, Inc.
- FEI Number: 3021769057
- City: Cypress
- State: California
- Country Name: United States
- Address Line 1: 6550 Katella Ave Ste 200
- Zip Code: 90630

## Related Documents

- [483 - iRhythm Technologies, Inc. - 2024-07-31](https://www.keypedia.com/records/483/irhythm-technologies-inc/23ef62b0-0b9d-4ee4-8036-8195e3210b79) — source: FDA, date: July 31, 2024
- [483 - iRhythm Technologies, Inc. - 2024-07-31](https://www.keypedia.com/records/483/irhythm-technologies-inc/0fcd49d0-47ef-4096-8d06-42760cad2e81) — source: FDA, date: July 31, 2024
- [483 - iRhythm Technologies, Inc. - 2024-07-31](https://www.keypedia.com/records/483/irhythm-technologies-inc/848b713d-9e33-4cc1-b651-5d975c2320f3) — source: FDA, date: July 31, 2024
- [FDA Inspection 1245153 - iRhythm Technologies, Inc. - 2024-07-31](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/197c534b-88c8-477e-856c-d772fce52ed2) — source: FDA, date: July 31, 2024
- [FDA Inspection 1245153 - iRhythm Technologies, Inc. - 2024-07-31](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/8bf2208c-c342-48d1-8196-d9826c28c05a) — source: FDA, date: July 31, 2024
- [483 - iRhythm Technologies, Inc. - 2022-08-12](https://www.keypedia.com/records/483/irhythm-technologies-inc/1f6b9f5b-915b-46ab-9ce1-83f72a64f8ce) — source: FDA, date: August 12, 2022
- [FDA Inspection 1178260 - iRhythm Technologies, Inc. - 2022-08-12](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/65f8441a-6cdc-4876-b42e-3c019a6a1fbb) — classification: Official Action Indicated (OAI), source: FDA, date: August 12, 2022
- [FDA Inspection 1178260 - iRhythm Technologies, Inc. - 2022-08-12](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/b9abf706-7515-42bc-8a09-1eb85ad30f80) — classification: Official Action Indicated (OAI), source: FDA, date: August 12, 2022
- [FDA Inspection 1077749 - iRhythm Technologies, Inc. - 2018-10-30](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/f4d166cd-3d08-4394-847c-105a7886d8b8) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2018
- [FDA Inspection 1077749 - iRhythm Technologies, Inc. - 2018-10-30](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/5a520e5d-e6e4-4abe-a6f3-59250e676dab) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2018
- [FDA Inspection 833835 - iRhythm Technologies, Inc. - 2013-05-24](https://www.keypedia.com/records/fda_inspections/irhythm-technologies-inc/ff2cdc6a-fc5a-4bfe-856f-e672c462eeb8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 24, 2013

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