FDA Inspection 1310990 — Santiago Ortega Gutierrez, M.D.

Santiago Ortega Gutierrez, M.D. — FEI 3031798440

The FDA completed an inspection of Santiago Ortega Gutierrez, M.D. on Mar 27, 2026 in Iowa City, IA. 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
Mar 27, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Iowa City, IA (United States)

Additional details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.