FDA Inspection 789741 — Abbott Ireland

Abbott Ireland — FEI 3002806284

The FDA completed an inspection of Abbott Ireland on June 21, 2012 in Sligo. 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
June 21, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sligo (Ireland)