{"@context":{"@vocab":"https://schema.org/"},"@type":"ItemList","@id":"https://api.morvs.ai/api/v1/fda/warning-letters/check?name=Ming%20Fai%20Industrial%20Co%20LTD","name":"Ming Fai Industrial 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":"2026-10-06T04:16:29.254Z"},"count":1,"matches":[{"id":"50fb8b2ac654681f","posted_date":"2023-11-14","letter_issue_date":"2023-06-01","company_name":"Ming Fai Industrial Co LTD","issuing_office":"Center for Devices and Radiological Health","subject":"CGMP/QSR/Medical Devices/Adulterated","canonical_url":"https://api.morvs.ai/fda-warning/50fb8b2ac654681f"}]}