{"@context":{"@vocab":"https://schema.org/"},"@type":"ItemList","@id":"https://api.morvs.ai/api/v1/fda/warning-letters/check?name=Marci%20Beauty%20LLC","name":"Marci Beauty LLC","_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":"2026-10-03T09:12:18.149Z"},"count":1,"matches":[{"id":"18660174cc0dc356","posted_date":"2021-10-05","letter_issue_date":"2021-02-02","company_name":"Marci Beauty LLC","issuing_office":"Center for Devices and Radiological Health","subject":"Investigational Device Exemptions (IDE)/Premarket Approval Application (PMA) Adulterated Device","canonical_url":"https://api.morvs.ai/fda-warning/18660174cc0dc356"}]}