FDA Inspection 1137406 — Rachel E. Sanborn, M.D.

Rachel E. Sanborn, M.D. — FEI 3017872104

The FDA completed an inspection of Rachel E. Sanborn, M.D. on February 24, 2021 in Portland, OR. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 24, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Portland, OR (United States)

Additional Details

Clinical Investigator (CI)