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FDA Inspection 1017658 — Abbott Laboratories GmbH

Abbott Laboratories GmbH — FEI 3002808216

The FDA completed an inspection of Abbott Laboratories GmbH on February 24, 2017 in Neustadt am Rubenberge. 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
February 24, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Neustadt am Rubenberge (Germany)

Facility

Other inspections at this facility

  • 1274874 (VAI Thu May 30 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1107966 (NAI Fri Aug 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 904481 (NAI Fri Oct 24 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 830369 (NAI Fri Apr 19 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 682154 (NAI Fri Jun 11 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources