FDA Inspection 722697 — Abbott Ireland

Abbott Ireland — FEI 3002806284

The FDA completed an inspection of Abbott Ireland on Apr 21, 2011 in Sligo. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 21, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sligo (Ireland)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.