NATCO Pharma (NSE:NATCOPHARM, BOM:524816) said the US Food and Drug Administration (FDA) concluded an inspection at its API manufacturing facility in Mekaguda, Hyderabad, India, according to a Friday filing on the Indian bourses.
The company received one observation in the Form 483 following the inspection, conducted from June 9 to June 13. NATCO said the observation was procedural in nature.