FDA Inspection 717041 — Abbvie Ireland NL B.V.

Abbvie Ireland NL B.V. — FEI 3004364014

The FDA completed an inspection of Abbvie Ireland NL B.V. on Mar 24, 2011 in Sligo. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 24, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sligo (Ireland)

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