FDA Inspection 1313860 — Jorge E. Lopera, M.D.

Jorge E. Lopera, M.D. — FEI 3042871494

The FDA completed an inspection of Jorge E. Lopera, M.D. on April 16, 2026 in San Antonio, TX. 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
April 16, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
San Antonio, TX (United States)

Additional Details

Clinical Investigator (CI)