{
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    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-10-05",
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      "advisory_committee_description": "Cardiovascular",
      "supplement_type": "30-Day Notice",
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      "expedited_review_flag": "N",
      "date_received": "2026-01-14",
      "decision_date": "2026-02-03",
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      "decision_code": "OK30",
      "ao_statement": "removal of redundant incoming inspection from certain qualified suppliers",
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