-- Aurobindo Pharma (NSE:AUROPHARMA, BOM:524804) has received a "voluntary action indicated" from the US Food and Drug Administration (US FDA) after the inspection of its oral solid dosage manufacturing unit in the Mahaboobnagar district of Telangana, India.
The inspection, which was conducted between Jan. 28 and Feb. 10, resulted in the US FDA issuing a 'Form 483' with nine observations, according to a Wednesday filing to the Indian stock exchanges.
With this classification, the inspection is now closed.
The company's shares were up over 3% in recent trade.