FDA Inspection 809009 — Raymond E. Tidman, MD

Raymond E. Tidman, MD — FEI 3003939497

The FDA completed an inspection of Raymond E. Tidman, MD on December 5, 2012 in Blue Ridge, GA. 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
December 5, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Blue Ridge, GA (United States)

Additional Details

Clinical Investigator (CI)