{"@context":{"@vocab":"https://schema.org/"},"@type":"ItemList","@id":"https://api.morvs.ai/api/v1/fda/warning-letters/check?name=Deymed%20Diagnostic%20s.r.o.","name":"Deymed Diagnostic s.r.o.","_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":"2026-10-06T02:26:49.732Z"},"count":1,"matches":[{"id":"017147ec92be88b0","posted_date":"2024-01-09","letter_issue_date":"2023-11-07","company_name":"Deymed Diagnostic s.r.o.","issuing_office":"\"OHT5: Office of Neurological and Physical Medicine Devices, Office of Product Evaluation and Quality\"","subject":"CGMP/QSR/Medical Devices/Adulterated","canonical_url":"https://api.morvs.ai/fda-warning/017147ec92be88b0"}]}