US FDA inspection at subsidiary Unit-II ends with one procedural observation
AUROPHARMA · price
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US FDA inspected Unit-II, an API manufacturing facility of Apitoria Pharma Private Limited (a wholly owned subsidiary of Aurobindo Pharma), located at Kazipally Industrial Area, Sangareddy District, Telangana, from September 7 to September 15, 2026. The inspection concluded with one procedural observation. The company will respond to the US FDA within the stipulated timeline and reaffirmed its commitment to quality and compliance standards.
Single procedural observation suggests no major compliance issues, supporting uninterrupted US market supplies and subsidiary operations.