FDA Inspection 843295 — Byrne, Timothy D.O

Byrne, Timothy D.O — FEI 3010306477

The FDA completed an inspection of Byrne, Timothy D.O on Jul 23, 2013 in Phoenix, AZ. 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
Jul 23, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Phoenix, AZ (United States)

Additional Details

Clinical Investigator (CI)