FDA Inspection 1127347 — Keila Hoover, M.D.

Keila Hoover, M.D. — FEI 3016483191

The FDA completed an inspection of Keila Hoover, M.D. on August 12, 2020 in Miami, FL. 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
August 12, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Miami, FL (United States)

Additional Details

Clinical Investigator (CI)