{"@context":{"@vocab":"https://schema.org/"},"@type":"ItemList","@id":"https://api.morvs.ai/api/v1/fda/warning-letters/check?name=YangZhou%20SuXiang%20Medical%20Instrument%20Co.%2C%20Ltd.","name":"YangZhou SuXiang Medical Instrument Co., Ltd.","_source":{"data_provider":"AI Analytics","brand_name":"MORVS","brand_url":"https://morvs.ai/","data_provider_url":"https://api.morvs.ai","license":"https://creativecommons.org/publicdomain/zero/1.0/","primary_source":"https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/compliance-actions-and-activities/warning-letters","generated_at":"2026-10-06T23:36:45.114Z"},"count":1,"matches":[{"id":"f67a4a37637339be","posted_date":"2024-07-16","letter_issue_date":"2024-07-08","company_name":"YangZhou SuXiang Medical Instrument Co., Ltd.","issuing_office":"Center for Drug Evaluation and Research (CDER)","subject":"CGMP/Finished Pharmaceuticals/Adulterated","canonical_url":"https://api.morvs.ai/fda-warning/f67a4a37637339be"}]}