Dr Reddy's claim of getting clearance after 8 observations from USFDA for Duvvada plant

As per the USFDA, Form 483 is issued to a firm's management at the conclusion of an inspection when the investigator has observed any conditions that in its judgment may constitute violations.

Dr Reddy's Laboratories Tuesday said US health regulator has issued eight observations after inspecting its formulations plant at Duvvada, Visakhapatnam.

"The audit of our formulations manufacturing facility at Duvvada, Visakhapatnam, by the US Food and Drug Administration (USFDA), has been completed today. We have been issued a Form 483 with eight observations, which we are addressing," the company said in a regulatory filing.

As per the USFDA, Form 483 is issued to a firm's management at the conclusion of an inspection when the investigator has observed any conditions that in its judgment may constitute violations of the Food Drug and Cosmetic (FD&C) Act and related Acts.

It notifies the company's management of objectionable conditions.

The Hyderabad-based company's shares today ended 2.48 per cent up at Rs 2,597.70 on the BSE.