FDA Inspection 580862 — James P. Johnston, CO

James P. Johnston, CO — FEI 1823996

The FDA completed an inspection of James P. Johnston, CO on May 1, 2009 in Michigan City, IN. 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
May 1, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Michigan City, IN (United States)