FDA 483 - Herbalife International of America, Inc - October 03, 2024

Herbalife International of America, Inc. in Winston Salem, NC, was inspected by the FDA, revealing deficiencies in their manufacturing records. The inspection found that the master manufacturing record lacked required corrective action plans, and batch production records were missing actual monitoring results and testing outcomes. These issues indicate a moderate level of non-compliance with good manufacturing practices for dietary supplements.