FDA Inspection 803895 — Abbott Ireland Limited

Abbott Ireland Limited — FEI 3008344661

The FDA completed an inspection of Abbott Ireland Limited on September 20, 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
September 20, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Sligo (Ireland)

Additional Details

Postmarket Audit Inspections