FDA Inspection 1199818 — Migvis Monduy, M.D.

Migvis Monduy, M.D. — FEI 3025365290

The FDA completed an inspection of Migvis Monduy, M.D. on March 9, 2023 in Orlando, FL. 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
March 9, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Orlando, FL (United States)

Additional Details

Clinical Investigator (CI)