FDA Inspection 1077749 — iRhythm Technologies, Inc.
The FDA completed an inspection of iRhythm Technologies, Inc. on October 30, 2018 in Cypress, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- October 30, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Cypress, CA (United States)