FDA WARNING_LETTER - JMT INTER LLC - September 23, 2025

The U.S. Food and Drug Administration (FDA) issued a warning letter to JMT Inter LLC, based in Middletown, Delaware, following a Foreign Supplier Verification Program (FSVP) inspection conducted from August 12 to September 23, 2025. This inspection followed previous evaluations in 2023 and 2024 to determine if the company was meeting safety requirements under the Federal Food, Drug, and Cosmetic Act. The FDA found that JMT Inter LLC failed to provide mandatory safety records despite multiple requests from investigators. Although the company claimed status as a "very small importer," it failed to provide documentation to verify this classification. Furthermore, the company did not produce safety verification records for imported soft drinks or provide written assurances that its foreign suppliers maintain public health standards equivalent to those required in the United States. To rectify these issues, JMT Inter LLC must respond within 15 working days with proof of their importer status and documentation showing that their suppliers meet U.S. safety protocols. Failure to comply may lead to the FDA refusing the entry of their products into the country or placing imported goods on a detention list.