Updates
This is to inform you that the US FDA has completed inspection of Company's formulations manufacturing facility (SEZ unit) located at Jadcherla, Telangana, India which was inspected between 24th July and 28th July 2017. The inspection has now been closed by the US FDA with one minor observation. The Company is in the process of submission of corrective and preventive action (CAPA) plan to the regulator within the stipulated timelines in response to the form 483 issued at the end of inspection.31-07-2017