FDA Inspection 705488 — CXR Company, Inc.

CXR Company, Inc. — FEI 3004034858

The FDA completed an inspection of CXR Company, Inc. on Jan 5, 2011 in Warsaw, 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
Jan 5, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Warsaw, IN (United States)