Piramal Pharma Achieves Successful Closure of US FDA Inspection at Kentucky Facility

Piramal Pharma Achieves Successful Closure of US FDA Inspection at Kentucky Facility

Piramal Pharma Achieves Successful Closure of US FDA Inspection at Kentucky Facility​

Piramal Pharma Ltd has confirmed the successful completion of its US FDA inspection at its manufacturing facility located in Lexington, Kentucky, USA. The successful conclusion was marked by the receipt of the Establishment Inspection Report (EIR) from the US FDA.

The company reported that the US FDA has issued the Establishment Inspection Report (EIR) for the Lexington facility. The report carries the classification of Voluntary Action Indicated (VAI).

The receipt of this EIR marks the successful closure of the inspection process for Piramal Pharma Ltd at the specified US location.

PPLPHARMA Stock Price Movement​

Shares of Piramal Pharma Limited are edging higher to ₹146.41 as of 10:22 AM today, gaining 0.29% in live trading. The stock activity remains robust, marked by a total volume of 764,138 shares traded so far in the session.

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Editorial Note

This news article was written and created by Karthik, and published on IST.
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