FDA Inspection 1243619 — Cheng Lun Soo, M.D.

Cheng Lun Soo, M.D. — FEI 3030483062

The FDA completed an inspection of Cheng Lun Soo, M.D. on Jun 26, 2024 in Oklahoma City, OK. 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
Jun 26, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Oklahoma City, OK (United States)

Additional Details

Clinical Investigator (CI)