483
Terence T. Sio, M.D., M.S.Terence T. Sio, M.D., M.S. – FDA 483, Mar 23, 2026
Record Details
An FDA inspection of Terence T. Sio, M.D., M.S., a clinical investigator in Phoenix, AZ, revealed one observation related to the conduct of a clinical study. The primary concern was the late reporting of Serious Adverse Events (SAEs) to the study sponsor, indicating a failure to follow the investigational plan. This suggests a moderate compliance issue in clinical trial oversight.
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