Cipla gets USFDA EIR for Indore facility
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Mumbai: Pharma major, Cipla, has recently announced that the Company has received Establishment Inspection Report (EIR) from the United States Food and Drug Administration (USFDA) for its Indore plant, indicating the closure of the inspection.
The inspection was conducted from 27th June 2022 to 1st July 2022.
"Further to the intimation dated 4th July 2022, this is to inform you that following the product-specific PreApproval Inspection (PAI) by the United States Food and Drug Administration (USFDA) at the Indore plant from 27th June 2022 to 1st July 2022, the Company has now received the Establishment Inspection Report (EIR) indicating closure of the inspection," the Company stated in a BSE filing,
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