USFDA inspection at Dr Reddy's FTO-11 facility ends with two Form 483 observations
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USFDA completed a Pre-Approval Inspection at Dr Reddy's FTO-11 manufacturing facility in Pydibhimavaram, Andhra Pradesh from October 5 to 7, 2026. The company received a Form 483 with two observations and will address them within the stipulated timeline.
Two observations are relatively minor and manageable; no warning letter or import alert reported. Investors should watch for further USFDA updates or approval delays linked to this site.