FDA Inspection 865230 — Abbott Ireland Limited

Abbott Ireland Limited — FEI 3008344661

The FDA completed an inspection of Abbott Ireland Limited on February 6, 2014 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
February 6, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sligo (Ireland)