FDA Inspection 1225756 — Demetrius K. Lopes, M.D.

Demetrius K. Lopes, M.D. — FEI 3004230403

The FDA completed an inspection of Demetrius K. Lopes, M.D. on December 11, 2023 in Park Ridge, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 11, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Park Ridge, IL (United States)

Additional Details

Clinical Investigator (CI)