Cadila Healthcare gets EIR from US FDA for Baddi facility
The United States Food and Drug Administration (US FDA) had conducted an inspection at the facility from July 15 to 19, 2019," Cadila Healthcare said
Drug firm Cadila Healthcare said its Baddi facility in Himachal Pradesh has received establishment inspection report (EIR) from the US health regulator. “The company’s formulations manufacturing facility located at Baddi, India, has received an EIR. The United States Food and Drug Administration (US FDA) had conducted an inspection at the facility from July 15 to 19, 2019,” Cadila Healthcare said in a filing to BSE.
The EIR report stated that the classification of the facility is ‘No Action Indicated (NAI)’, it added.
Shares of Cadila Healthcare were trading at Rs 252.35 per scrip on BSE, up 0.96 per cent from its previous close.
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