Hikal Gujarat facility gets EIR from USFDA
The pharmaceutical manufacturing facility at Panoli in Gujarat was recently inspected by the US Food and Drug Administration (USFDA) in compliance with their requirements.
New Delhi: Drug firm, Hikal recently announced that the US Health regulator has issued an Establishment Inspection Report (EIR) for its facility at Panoli, Gujarat.
The pharmaceutical manufacturing facility at Panoli in Gujarat was recently inspected by the US Food and Drug Administration (USFDA) in compliance with their requirements.
The five-day detailed inspection was carried out during the period September 9-13 this year, the company said in its BSE filing.
Also Read: Hikal up 11 pc on successful USFDA inspection
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