FDA Inspection 846345 — Roberto Giugliani, MD, PhD

Roberto Giugliani, MD, PhD — FEI 3010223469

The FDA completed an inspection of Roberto Giugliani, MD, PhD on Aug 2, 2013 in Porto Alegre. 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
Aug 2, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Porto Alegre (Brazil)

Additional Details

Clinical Investigator (CI)

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