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Granules India’s arm gets EIR from USFDA for Virginia facility

29 Nov 2019 Evaluate

US Food and Drug Administration (USFDA) has issued Establishment Inspection Report (EIR) for Granules Pharmaceuticals, Inc. facility, a wholly-owned foreign subsidiary of Granules India, located in Chantilly, Virginia, USA.

This facility was inspected by USFDA in August 2019 and there were two minor observations during the inspection. The company has responded to the observations within the stipulated timeframe.

Granules India is manufacturer and supplier of pharmaceutical products. Its products include active pharmaceutical ingredients (API) like tablets, caplets, rapid release, pharmaceutical, formulation intermediates (PFI) and Finished Dosages (FDs).

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