Granules India has received the Establishment Inspection Report (EIR) from the USFDA for the inspection conducted at its Jeedimetla facility in December 2015.
The USFDA has acknowledged receipt of its responses sent on January 7 and March 28, 2016 on the observations issued by it for the Jeedimetla facility. The USFDA closed the matter and issued EIR for the Jeedimetla facility situated in the state of Telangana.
Granules India produces Finished Dosages (FDs), Pharmaceutical Formulation Intermediates (PFIs) and Active Pharmaceutical Ingredients (APIs) for quality conscious customers in the regulated and semi-regulated markets.
