Qvents

Qvents

Discussion forum for Pharma Quality events, Regulatory Actions

Warning letters, 483s, Recalls, Import Alerts, Audit observations

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Aarti Drugs USFDA 483 Flags Unique Chall

Aarti Drugs API facility in Tarapur, India was inspected by USFDA investigators Rajeev R. Srivastava

Yiling Pharma Warning Letter: Equipment

The U.S. Food and Drug Administration (FDA) has issued a Warning Letter in June 2025

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