FDA Inspection 961084 — Edward Loftus

Edward Loftus — FEI 3012080069

The FDA completed an inspection of Edward Loftus on Mar 4, 2016 in Rochester, MN. 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
Mar 4, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rochester, MN (United States)

Additional Details

Clinical Investigator (CI)