Granules India’s Vizag facility completes US FDA inspection with zero 483 observations

This facility manufactures APIs and formulations of oncology and non-oncology products

Granules India’s Unit V facility located at Anakapally, Visakhapatnam, Andhra Pradesh, India has successfully completed the US Food and Drug Administration (FDA) inspection between April 8-12 2024, resulting in zero 483 observations.

This audit was a Pre-Approval Inspection (PAI) and cGMP audit for Active Pharmaceutical Ingredients (APIs) and Formulations (FDs) for oncology and non-oncology products.

483 observationscGMP auditGranules IndiaUS FDAUS FDA inspectionVisakhapatnam
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