FDA Inspection 1247049 — Mark Delegge, M.D.

Mark Delegge, M.D. — FEI 3030582530

The FDA completed an inspection of Mark Delegge, M.D. on Aug 9, 2024 in Durham, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 9, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Durham, NC (United States)

Additional Details

Clinical Investigator (CI)