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FDA Inspection 1071110 — Jonathan E. Greenleaf, MD

Jonathan E. Greenleaf, MD — FEI 3014698689

The FDA completed an inspection of Jonathan E. Greenleaf, MD on Oct 16, 2018 in Tigard, OR. 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
Oct 16, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tigard, OR (United States)

Additional details

Clinical Investigator (CI)

Facility

FDA data resources

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