The company has received the EIR from the United States Food and Drug Administration (USFDA) on successful inspection closure for the post-marketing adverse drug experience reporting inspection (PADE) conducted at Nungambakkam, Chennai facility, Orchid Pharma said in a BSE filing.
"The facility was inspected by USFDA in the month of June, 2017, it added.
As per the USFDA, after the completion of an inspection of a facility, an EIR is issued to a company detailing inspectional findings.
Shares of Orchid Pharma today closed 4.93 per cent higher at Rs 23.40 per scrip on BSE.
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