FDA Inspection 1078972 — Robert Norman Harden

Robert Norman Harden — FEI 3014506803

The FDA completed an inspection of Robert Norman Harden on Dec 6, 2018 in Chicago, IL. 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
Dec 6, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Chicago, IL (United States)

Additional Details

Sponsor-Investigator (S-I)