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    Cadila Healthcare gets EIR report on Ahmedabad SEZ facility

    Medical Dialogues BureauWritten by Medical Dialogues Bureau   |  

    New Delhi: Drug firm Cadila Healthcare Monday said it has received establishment inspection report from the US health regulator with voluntary action indicated (VAI) classification for its Ahmedabad SEZ facility.


    The United States Food and Drug Administration (USFDA) had conducted an inspection of the company's formulations manufacturing facility located at SEZ, Ahmedabad from March 25 to April 3, 2019, Cadila Healthcare said in a BSE filing.


    Read Also: Cadila Healthcare gets 11 USFDA observations for St Louis facilities

    The plant has received an establishment inspection report (EIR). The EIR report stated that the classification of the facility is VAI, it added.


    As per the USFDA, VAI means that though "objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action".


    Read Also: Cadila Healthcare posts Q4 net profit of Rs 460 crore


    BSECadila Ahmedabad SEZ facilityCadila HealthcareDrug firm Cadila HealthcareEIREstablishment Inspection ReportShares of Cadila HealthcareUnited States Food and Drug AdministrationUS healthUSFDAVAIVoluntary Action Indicated
    Source : Cadila Healthcare

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    Medical Dialogues Bureau
    Medical Dialogues Bureau

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