FDA Inspection 861321 — AbbVie Inc.

AbbVie Inc. — FEI 3009751352

The FDA completed an inspection of AbbVie Inc. on Dec 13, 2013 in North Chicago, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 13, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
North Chicago, IL (United States)