FDA Inspection 1302550 — Jason Pope, MD

Jason Pope, MD — FEI 3041324906

The FDA completed an inspection of Jason Pope, MD on Jan 26, 2026 in Santa Rosa, CA. 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
Jan 26, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Santa Rosa, CA (United States)

Additional details

Clinical Investigator (CI)

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