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Zydus Lifesciences receives EIR from US FDA for Moraiya facility

Zydus Lifesciences receives EIR from US FDA for Moraiya facility

Zydus Lifesciences has announced the receipt of an Establishment Inspection Report (EIR) from the United States Food and Drug Administration (USFDA) for its formulations manufacturing facility in Moraiya, near Ahmedabad.

As per the filing, the USFDA has determined that the inspection classification of the facility is Voluntary Action Indicated (VAI).

The US FDA inspected the facility from July 26 to August 5, 2022, which concluded with four observations. The US FDA has indicated that the inspection is closed.
Read more on:
EIR US FDA Zydus Lifesciences
More news about: quality / gmp | Published by Sudeep Soparkar | November - 07 - 2022 | 849

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