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Sun Pharma update on USFDA inspection of its Dadra facility

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Receives copy of EIR from USFDA

Sun Pharmaceuticals Industries has received a communication from the US FDA releasing a copy of the Establishment Inspection Report (EIR) in respect of the inspection of Company's Dadra facility. Earlier, the USFDA had issued Form- 483 observation letter post inspection completed on 13 April 2017.

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(This story has not been edited by Business Standard staff and is auto-generated from a syndicated feed.)

First Published: Wed, October 11 2017. 19:56 IST
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