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Dr Reddy's Laboratories receives EIR for its API manufacturing plant at Miryalaguda

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Capital Market

From USFDA

Dr Reddy's Laboratories has received an Establishment Inspection Report from the USFDA following closure of audit of its API manufacturing plant at Miryalaguda. The Company was issued a form 483 with three observations subsequent to the audit of the said unit in February 2017.

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First Published: Jun 14 2017 | 9:29 AM IST

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