{"@context":{"@vocab":"https://schema.org/"},"@type":"ItemList","@id":"https://api.morvs.ai/api/v1/fda/warning-letters/check?name=AMCO%20International%20Manufacturing%20%26%20Design%2C%20Inc.","name":"AMCO International Manufacturing & Design, Inc.","_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":"2026-10-05T16:42:25.117Z"},"count":1,"matches":[{"id":"e6c2e8066f7107e7","posted_date":"2024-07-30","letter_issue_date":"2024-06-25","company_name":"AMCO International Manufacturing & Design, Inc.","issuing_office":"Center for Devices and Radiological Health","subject":"Unapproved Device Violation","canonical_url":"https://api.morvs.ai/fda-warning/e6c2e8066f7107e7"}]}