FDA Inspection 1240183 — Matthew A. Powell, M.D.

Matthew A. Powell, M.D. — FEI 3030691560

The FDA completed an inspection of Matthew A. Powell, M.D. on Jun 3, 2024 in Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 3, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Saint Louis, MO (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
2272821 CFR 312.64(b)Safety Reports - Non-Serious Events