Dr Reddy's Labs Srikakulam facility gets EIR from USFDA
Written By : Ruchika Sharma
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2025-10-22 06:00 GMT | Update On 2025-10-22 06:00 GMT
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Hyderabad: Dr Reddy's Labs has announced that the Company has received the Establishment Inspection Report (EIR) from the United States Food & Drug Administration (USFDA) for its formulations manufacturing facility FTO 11 in Srikakulam, Andhra Pradesh, India.
The USFDA has classified the inspection outcome as 'Voluntary Action Indicated (VAI)' and concluded that the inspection is officially closed under 21 CFR 20.64(d)(3).
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