FDA Inspection 1088122 — Robert Anderson

Robert Anderson — FEI 3014932055

The FDA completed an inspection of Robert Anderson on April 12, 2019 in Omaha, NE. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 12, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Omaha, NE (United States)

Additional Details

Clinical Investigator (CI)