FDA Inspection 1002823 — Goddard, Dr James K

Goddard, Dr James K — FEI 3011520910

The FDA completed an inspection of Goddard, Dr James K on January 17, 2017 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 17, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Saint Paul, MN (United States)

Additional Details

Clinical Investigator (CI)