FDA Inspection 1141571 — Keila Hoover, M.D.

Keila Hoover, M.D. — FEI 3016483191

The FDA completed an inspection of Keila Hoover, M.D. on Apr 29, 2021 in Miami, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 29, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Miami, FL (United States)

Additional Details

Clinical Investigator (CI)

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