FDA Inspection 1113141 — Raymond E. Tidman, MD

Raymond E. Tidman, MD — FEI 3003939497

The FDA completed an inspection of Raymond E. Tidman, MD on December 4, 2019 in Blue Ridge, GA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 4, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Blue Ridge, GA (United States)

Additional Details

Clinical Investigator (CI)