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Dr. Reddy's Laboratories Limited's API facility at Srikakulam completes USFDA inspection successfully

Dr. Reddy's Laboratories Limited's API facility at Srikakulam completes USFDA inspection successfully

The United States Food & Drug Administration (USFDA) today completed a Pre-Approval Inspection (PAI) and a routine GMP inspection at Dr. Reddy's Laboratories Limited'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).
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Dr Reddy Laboratories NAI USFDA
More news about: quality / gmp | Published by Sudeep Soparkar | July - 20 - 2023 | 977

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