FDA Inspection 1118427 — Covidien, LP

Covidien, LP — FEI 1219930

The FDA completed an inspection of Covidien, LP on February 28, 2020 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 28, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
North Haven, CT (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures