The US Food & Drug Administration (USFDA) has completed the inspection at Alkem Laboratories’ St Louis facility. The regulator had conducted an inspection at the company’s manufacturing facility located at St Louis, USA from October 23, 2017 to October 27, 2017. At the end of the inspection, no Form 483 was issued.
Alkem Laboratories is a leading Indian pharmaceutical company with global operations, engaged in the development, manufacture and sale of pharmaceutical and nutraceutical products. The company produces branded generics, generic drugs, active pharmaceutical Ingredients (APIs) and nutraceuticals, which it markets in India and International markets.