Development · 18 Aug 2026
AUROPHARMA, full dossier1 publisher has reported this development. Each act of reporting is below, cited.
Aurobindo Pharma's Raleigh Plant in North Carolina received an Establishment Inspection Report from the US FDA and was classified as 'Voluntary Action Indicated' following an inspection from March 24 to April 10, 2025 that resulted in a Form 483 with 11 observations.
A single act of reporting so far, corroborating sources join this record as they publish.
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