FDA Inspection 900524 — Covidien

Covidien — FEI 3003495548

The FDA completed an inspection of Covidien on August 22, 2014 in San Isidro. 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
August 22, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
San Isidro (Dominican Republic (the))