Dr Reddy's Laboratories on Thursday said it has received an establishment inspection report (EIR) from the US health regulator for its Nalgonda-based active pharmaceutical ingredient (API) manufacturing unit.
"With regard to the audit of our API manufacturing plant 5 at Miryalaguda, Nalgonda district, Telangana, we would like to inform you that we have received the EIR from the USFDA, for the above-referred facility, indicating closure of the audit," the Hyderabad-based company said in a regulatory filing.
The inspection classification of this facility is determined as "voluntary action indicated" (VAI), it added.
USFDA issues an EIR to a company when an inspection is satisfactorily closed.
Disclaimer: No Business Standard Journalist was involved in creation of this content
