Unichem Laboratories’ Ghaziabad facility receives EIR from USFDA

07 Jun 2017 Evaluate

Unichem Laboratories has received an Establishment Inspection Report (EIR) from the United States Food & Drug Administration (USFDA) for its formulations manufacturing facility at Ghaziabad.

This receipt indicates the successful closure of the inspection and the queries raised during the audit (Form 483). The inspection has now been closed by the USFDA. The inspection was carried out between February 24, 2017 to March 3, 2017.

Unichem Laboratories is an international, integrated, specialty pharmaceutical company. It manufactures and markets a large basket of pharmaceutical formulations as branded generics as well as generics in India and several other markets across the world.

 

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