FDA Inspection 1093003 — Richard F. Harty, M.D.

Richard F. Harty, M.D. — FEI 3014721885

The FDA completed an inspection of Richard F. Harty, M.D. on May 16, 2019 in Oklahoma City, OK. 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
May 16, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Oklahoma City, OK (United States)

Additional Details

Clinical Investigator (CI)