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FDA Inspection 727883 — Covidien, LP

Covidien, LP — FEI 1219930

The FDA completed an inspection of Covidien, LP on June 16, 2011 in North Haven, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 16, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
North Haven, CT (United States)

Facility

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  • 812526 (NAI Thu Dec 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 767957 (OAI Thu Feb 09 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources