FDA Inspection 1042339 — Aclan Dogan, MD

Aclan Dogan, MD — FEI 3013909375

The FDA completed an inspection of Aclan Dogan, MD on November 21, 2017 in Portland, OR. 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
November 21, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Portland, OR (United States)

Additional Details

Clinical Investigator (CI)