FDA Inspection 796052 — Abbott Ireland Diagnostics Division

Abbott Ireland Diagnostics Division — FEI 3005094123

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

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