FDA Inspection 1245190 - iRhythm Technologies Inc - July 31, 2024

FDA Inspection 1245190 for iRhythm Technologies Inc on July 31, 2024. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 1245190 for iRhythm Technologies Inc on July 31, 2024. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 803.50(a)(2)

21 CFR 820.100(a)

21 CFR 820.30(g)

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Record Information

Company

iRhythm Technologies Inc

Inspection Date

July 31, 2024

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: bee72d5f-6c26-4e0f-b651-273d18bd14ff

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