USFDA concludes inspection at Dr Reddy's Labs Srikakulam facility with zero observations
The inspection closed with zero observations and a classification of No Action Indicated.;
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Hyderabad: Pharma major, Dr Reddy's Labs, has announced that the United States Food & Drug Administration (USFDA) has completed a Pre-Approval Inspection (PAI) and a routine GMP inspection at the company's API manufacturing facility in Srikakulam, Andhra Pradesh, India (CTO-6).
The inspection was conducted from 10th July, 2023 to 19th July, 2023.
"The inspection closed with zero observations and a classification of No Action Indicated (NAI)," the company informed in a BSE filing.
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