FDA Inspection 611151 — Control Devices - Carr Lane

Control Devices - Carr Lane — FEI 1937613

The FDA completed an inspection of Control Devices - Carr Lane on Sep 14, 2009 in Saint Louis, MO. 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
Sep 14, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)