Liuzhou Liangmianzhen (LMZ) Co., Ltd. – FDA 483, Mar 22, 2024
An FDA inspection of Liuzhou Liangmianzhen (LMZ) Co., LTD. in Liuzhou, China, an OTC drug manufacturer, identified significant deficiencies in laboratory controls, equipment maintenance, and environmental monitoring. The firm failed to implement scientifically sound testing procedures, maintain equipment and water systems properly, and establish adequate controls to prevent microbial contamination. These issues indicate a lack of adherence to good manufacturing practices, posing potential risks to drug product quality and safety.
ID · 95024277-3c74-45f9-855f-5b65a122eec2
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.