US FDA inspection at Auro Peptides completed with single observation
AUROPHARMA · price
▲ positive · ▼ negative · ● neutral filings · teal = economic event · numbered = multiple that day (click to pick). Times IST.
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US FDA conducted a routine inspection at Auro Peptides Ltd, Aurobindo Pharma's subsidiary that makes Peptide APIs in Telangana, from August 17 to 21, 2026. The inspection ended with only one observation related to facility and equipment maintenance, with no data integrity or GMP compliance issues. Corrective action was already started during the inspection, and a formal response will be sent within the required timeline.
Positive. A single minor observation with no data integrity or GMP concerns reaffirms manufacturing compliance at the subsidiary.