FDA Inspection 658985 — John G. Anderson, M.D.

John G. Anderson, M.D. — FEI 3008231615

The FDA completed an inspection of John G. Anderson, M.D. on April 26, 2010 in Grand Rapids, MI. 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
April 26, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Grand Rapids, MI (United States)

Additional Details

Clinical Investigator (CI)