USFDA inspection at Bengaluru facility ends with one observation
ONESOURCE · price
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USFDA conducted a routine cGMP inspection at OneSource Specialty Pharma's Sterile Product Division facility in Bengaluru from June 22 to June 30, 2026. The inspection concluded with one observation. The company will respond comprehensively to the FDA within the stipulated timeframe and will update stock exchanges on further developments.
Single observation is generally manageable; outcome of company response and any FDA classification will determine impact on US business.