FDA Inspection 609286 — Barry K Rayburn MD

Barry K Rayburn MD — FEI 3007211388

The FDA completed an inspection of Barry K Rayburn MD on Aug 26, 2009 in Birmingham, AL. 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
Aug 26, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Birmingham, AL (United States)

Additional Details

Clinical Investigator (CI)