FDA Inspection 1281522 — Roberto Giugliani, MD, PhD

Roberto Giugliani, MD, PhD — FEI 3010223469

The FDA completed an inspection of Roberto Giugliani, MD, PhD on Sep 2, 2025 in Porto Alegre. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 2, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Porto Alegre (Brazil)

Additional Details

Clinical Investigator (CI)

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