US FDA closes inspection of Dr. Reddy's Srikakulam unit with VAI tag

The US FDA has classified Dr. Reddy's Laboratories' Srikakulam facility in Andhra Pradesh as Voluntary Action Indicated and closed the inspection. The regulator had issued a Form 483 with three observations after inspecting the unit from July 20 to 29. VAI means objectionable conditions were found, but no regulatory or administrative action is recommended.