Drug firm Glenmark has received establishment inspection report (EIR) from the US health regulator on closure of inspection of its Ankleshwar plant in Gujarat, the company said today.
"Glenmark would like to state that its Ankleshwar plant received the EIR (establishment inspection report) yesterday.
The EIR is issued by the FDA only if it finds the facility to be deemed acceptable," it said in a BSE filing.
The USFDA releases a copy of the EIR to the establishment that is the subject of an FDA or FDA-contracted inspection when the agency determines the inspection to be closed.
Glenmark was clarifying to the stock exchanges over a news report which claimed that its Ankleshwar plant received observations from the USFDA during its inspection in December 2016.
The stock was trading at Rs 905, up 1.58 percent from its previous close on BSE.
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