Mumbai, Aug. 22 -- In a regulatory filing made post market hours yesterday, the pharmaceutical major said that the US FDA had conducted an inspection at the company's FDF manufacturing plant located in Parawada, Visakhapatnam, Andhra Pradesh, India, which was conducted from 17th August 2026 to 21st August 2026.

Upon conclusion of the inspection, the c ompany has been issued a Form 483 with four observations.

"The company believes that the observations are procedural in nature and is confident of addressing these observations comprehensively within stipulated timelines," NATCO Pharma said in a statement.

NATCO Pharma develops, manufactures and distributes generic and branded pharmaceuticals, specialty pharmaceuticals, active pharma ingr...