FDA Inspection 792561 — Covidien LP

Covidien LP — FEI 1282497

The FDA completed an inspection of Covidien LP on July 20, 2012 in Mansfield, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 20, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mansfield, MA (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints