FDA Inspection 796052 — Abbott Ireland Diagnostics Division

Abbott Ireland Diagnostics Division — FEI 3005094123

The FDA completed an inspection of Abbott Ireland Diagnostics Division on August 30, 2012 in Co. Longford. 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
August 30, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Co. Longford (Ireland)