FDA Inspection 1231776 — Albert Oriol Rocafiguera, MD

Albert Oriol Rocafiguera, MD — FEI 3009025637

The FDA completed an inspection of Albert Oriol Rocafiguera, MD on February 22, 2024 in Badalona. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 22, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Badalona (Spain)

Additional Details

Clinical Investigator (CI)