FDA Inspection 873392 — Mark J Goodwin, MD

Mark J Goodwin, MD — FEI 3010747418

The FDA completed an inspection of Mark J Goodwin, MD on Apr 1, 2014 in Naperville, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 1, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Naperville, IL (United States)

Additional Details

Clinical Investigator (CI)