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FDA Inspection 1255834 — Covidien, LP

Covidien, LP — FEI 1219930

The FDA completed an inspection of Covidien, LP on November 21, 2024 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 21, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
North Haven, CT (United States)

Facility

Other inspections at this facility

  • 1118427 (VAI Fri Feb 28 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 891371 (NAI Thu Aug 14 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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))
  • 727883 (VAI Thu Jun 16 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources