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FDA Inspection 1012249 — Abbvie Biotechnology Ltd.

Abbvie Biotechnology Ltd. — FEI 3004620772

The FDA completed an inspection of Abbvie Biotechnology Ltd. on April 28, 2017 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
April 28, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Barceloneta, PR (United States)

Facility

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  • 1084057 (VAI Mon Mar 25 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1055102 (VAI Fri Jun 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 969277 (VAI Thu Mar 24 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 887947 (VAI Wed Jul 16 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources