FDA 483 - Tailift Co., Ltd.

An FDA inspection of Tailift Co. Ltd. in Nantou, Taiwan, revealed deficiencies related to the safety and labeling of Class 4 laser products. Observations included a Class 4 laser system being operable with the key removed and the absence of required warning labels for Class 4 laser products and defeatably interlocked protective housings. The firm initiated corrective actions during the inspection and committed to addressing the remaining issues.