FDA 483 - Xi'an Livingbond Nonwoven Products Corp., Ltd. - January 07, 2019

X'ian Livingbond Nonwoven Products Corp., Ltd. received a Form FDA 483 following an inspection of their OTC Topical Drug Manufacturer facility in Xian, China. The inspection revealed significant deficiencies across various aspects of their operations, including inadequate product testing, lack of process validation, insufficient laboratory controls, and poor documentation practices. These observations indicate a general lack of adherence to current good manufacturing practices, impacting product quality and control.