FDA Inspection 668310 — Covidien

Covidien — FEI 3002807850

The FDA completed an inspection of Covidien on May 27, 2010 in Galway. 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 27, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Galway (Ireland)