FDA Inspection 1070730 — Roberto Hegg

Roberto Hegg — FEI 3009399569

The FDA completed an inspection of Roberto Hegg on Sep 20, 2018 in Sao Paulo. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 20, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Sao Paulo (Brazil)

Additional Details

Clinical Investigator (CI)