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Unichem Laboratories receives EIR from USFDA for Roha API facility
Aug-26-2025

Unichem Laboratories has received the Establishment Inspection Report (EIR) from United States Food and Drug Administration (USFDA) for its Roha API facility. The USFDA had conducted an inspection at the company’s Roha API facility from June 16, 2025 to June 20, 2025. USFDA has classified the inspection as Voluntary Action Initiated (VAI).

Unichem Laboratories is engaged in manufacturing formulations, pharmaceuticals and active pharmaceutical ingredients (APIs).

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