FDA Inspection 1003229 — Howard S. Barnebey, MD

Howard S. Barnebey, MD — FEI 3012985905

The FDA completed an inspection of Howard S. Barnebey, MD on Feb 7, 2017 in Bellevue, WA. 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
Feb 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Bellevue, WA (United States)

Additional Details

Clinical Investigator (CI)

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