FDA Inspection 1304768 — Demetri W. Marshall, M.D.

Demetri W. Marshall, M.D. — FEI 3041916301

The FDA completed an inspection of Demetri W. Marshall, M.D. on Feb 20, 2026 in Fayette, MS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
Feb 20, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Fayette, MS (United States)

Additional Details

Clinical Investigator (CI)