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      "text": "While the FDA's findings are “known” to many investors today, we believe that reviewing the multi-year fact pattern in totality produces an extremely unfavorable view of management's actions. We believe iRhythm management continually delayed and downplayed its disclosure of its regulatory troubles...",
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      "text": "In May 2023, iRhythm disclosed it had received a Department of Justice subpoena, the subject of which was later revealed to be the Zio AT issues. As stated in an iRhythm petition, the “Government issued a Subpoena with thirty-two requests...",
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      "text": "Following a simultaneous inspection of both iRhythm facilities in July 2024, we believe a clear sign of government distrust, iRhythm received two additional Form 483s. Once again, the FDA found that iRhythm jeopardized patient safety, this time by failing to investigate, report, and remediate over 4,000 complaints related to patient data reporting errors and data measurement and algorithm mistakes...",
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      "text": "Government issued a Subpoena with thirty-two requests—ranging in subject matter from quality control policies, to scientific studies, to coverage and reimbursement by federal and state healthcare — iRhythm petition",
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