FDA Inspection 1211212 — James S. Jenkins, M.D.

James S. Jenkins, M.D. — FEI 3027033876

The FDA completed an inspection of James S. Jenkins, M.D. on July 20, 2023 in New Orleans, LA. 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
July 20, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
New Orleans, LA (United States)

Additional Details

Clinical Investigator (CI)