FDA Inspection 930720 — Albert Oriol Rocafiguera, MD

Albert Oriol Rocafiguera, MD — FEI 3009025637

The FDA completed an inspection of Albert Oriol Rocafiguera, MD on May 22, 2015 in Badalona. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 22, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Badalona (Spain)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
752621 CFR 312.62(a)Accountability records
756021 CFR 312.60FD-1572, protocol compliance