The US Food and Drug Administration (USFDA) has completed inspection at Alkem Laboratories’ Bioequivalence Center located at Taloja, Maharashtra. The agency had conducted inspection from October 14, 2019 to October 18, 2019. 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.