{"@context":{"@vocab":"https://schema.org/"},"@type":"ItemList","@id":"https://api.morvs.ai/api/v1/fda/warning-letters/check?name=Brenntag%20Great%20Lakes%2C%20LLC","name":"Brenntag Great Lakes, 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":"2026-10-04T22:43:53.592Z"},"count":1,"matches":[{"id":"b22ac9184822f8c5","posted_date":"2023-11-21","letter_issue_date":"2023-10-26","company_name":"Brenntag Great Lakes, LLC","issuing_office":"Division of Pharmaceutical Quality Operations III","subject":"CGMP/Finished Pharmaceuticals/Adulterated","canonical_url":"https://api.morvs.ai/fda-warning/b22ac9184822f8c5"}]}