Dr Reddy’s Laboratories gets USFDA’s EIR to API plant in Telangana

The US Food and Drug Administration has given an 'establishment inspection report' to the company after inspection of Dr Reddy Laboratories active pharmaceutical ingredients (API) unit at Miryalaguda in Telangana

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New Delhi: Dr Reddy’s Laboratories in its recent filing to the National Stock Exchange (NSE) broke the news that company has received an establishment inspection report (EIR) from the USFDA on 16th June as the closure of audit for the above-referred facility.
The company has said that the US Food and Drug Administration, which inspected active pharmaceutical ingredients (API) unit at Miryalaguda in Telangana in March this year, has given an ‘establishment inspection report’.
Earlier on February 21, the company had informed that the FDA had issued form 483 with three observations.
“In that regard, we would now like to inform you that we have received an establishment inspection report (EIR) from the USFDA as the closure of audit for the above-referred facility,” the drug maker said its filing.
After the news broke out, the company’s stock was trading at Rs 2,679.70, up nearly 2 percent.
According to information provided by the FDA in its website, if no enforcement action is contemplated, or after enforcement action is concluded, the drug regulator provides inspected establishments with a final inspection report, called an EIR.
The EIR includes the brief history of prior inspectional findings, including any action taken by FDA or corrective action taken by the firm in response to a previous inspection, the investigator’s narrative report, any refusals, voluntary corrections, or promises made by the firm’s management and copies of forms the FDA issued to the firm during the inspection, including the FDA form 483.