FDA Inspection 1299372 — Albert Oriol Rocafiguera, MD

Albert Oriol Rocafiguera, MD — FEI 3009025637

The FDA completed an inspection of Albert Oriol Rocafiguera, MD on December 5, 2025 in Badalona. 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
December 5, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Badalona (Spain)

Additional Details

Clinical Investigator (CI)