FDA Inspection 1295370 — Kamran Muhammad, MD

Kamran Muhammad, MD — FEI 3040059574

The FDA completed an inspection of Kamran Muhammad, MD on December 5, 2025 in Tulsa, OK. 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 5, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tulsa, OK (United States)

Additional Details

Clinical Investigator (CI)