Dr Reddys Laboratories receives EIR for its facility at Bachupally, Hyderabad

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Last Updated : Dec 12 2017 | 12:31 PM IST

From USFDA

Dr Reddys Laboratories has received an Establishment Inspection Report from the USFDA on 11 December 2017 following closure of audit of its Formulations Manufacturing Plant 3 at Bachupally, Hyderabad by the USFDA, where in the Company received a Form 483 with 11 observations.

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First Published: Dec 12 2017 | 12:10 PM IST

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