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 or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Drugs.