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FDA Inspection 981552 — AbbVie Ltd

AbbVie Ltd — FEI 3000210838

The FDA completed an inspection of AbbVie Ltd on July 29, 2016 in Barceloneta, PR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 29, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Barceloneta, PR (United States)

Facility

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  • 1081767 (NAI Fri Dec 21 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 879731 (VAI Tue May 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 774513 (VAI Thu Mar 29 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources