FDA Inspection 907256 — AbbVie Inc

AbbVie Inc — FEI 3010757606

The FDA completed an inspection of AbbVie Inc on December 16, 2014 in North Chicago, IL. 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
December 16, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
North Chicago, IL (United States)