FDA Inspection 973363 — Abbott Ireland

Abbott Ireland — FEI 3002806284

The FDA completed an inspection of Abbott Ireland on May 24, 2016 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
May 24, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Sligo (Ireland)