FDA Inspection 1150615 — Smitha Reddy, M.D.

Smitha Reddy, M.D. — FEI 3017760842

The FDA completed an inspection of Smitha Reddy, M.D. on August 20, 2021 in Poway, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 5 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 20, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Poway, CA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
723121 CFR 50.20Consent not obtained, exceptions do not apply
749821 CFR 312.66Unanticipated problems
752621 CFR 312.62(a)Accountability records
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance