Global pharma primary Lupin received the Establishment Inspection Report (EIR) from the United States Food and Drug Administration (USFDA) for its Nagpur Unit-1 production facility that manufactures oral strong dosage bureaucracy. The EIR changed into issued publish the ultimate inspection of the facility carried out in July 2023.
The USFDA has determined that the inspection classification of the facility is Voluntary Action Indicated (VAI).
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