FDA Inspection 699834 — Covidien, LP

Covidien, LP — FEI 1219930

The FDA completed an inspection of Covidien, LP on November 8, 2010 in North Haven, CT. 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
November 8, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
North Haven, CT (United States)

Additional Details

Sponsor, Contract Research Organization