FDA Inspection 803895 — Abbott Ireland Limited

Abbott Ireland Limited — FEI 3008344661

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

Additional Details

Postmarket Audit Inspections

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