FDA Inspection 1027866 — Marco Antonio Alvarez Gonzalez, MD, PhD

Marco Antonio Alvarez Gonzalez, MD, PhD — FEI 3013615207

The FDA completed an inspection of Marco Antonio Alvarez Gonzalez, MD, PhD on Sep 15, 2017 in Barcelona. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Sep 15, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Barcelona (Spain)

Additional details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.