FDA Inspection 1117681 — Alberto Aliaga Verdugo, M.D.

Alberto Aliaga Verdugo, M.D. — FEI 3015874037

The FDA completed an inspection of Alberto Aliaga Verdugo, M.D. on January 24, 2020 in Sevilla. 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
January 24, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Sevilla (Spain)

Additional Details

Clinical Investigator (CI)