FDA 483 - Herbalife International of America, Inc - July 03, 2019

An FDA inspection of Herbalife International of America in Winston Salem, NC, revealed significant deficiencies in the firm's manufacturing practices. Observations included a lack of a corrective action plan for out-of-specification cleaning results, failure to follow written cleaning procedures for equipment, and improper use of cleaning compounds. These issues indicate a failure to maintain adequate control over sanitation and equipment hygiene.