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FDA Inspection 548334 — Abbott Laboratories GmbH

Abbott Laboratories GmbH — FEI 3002808216

The FDA completed an inspection of Abbott Laboratories GmbH on October 14, 2008 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
October 14, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Neustadt am Rubenberge (Germany)

Facility

Other inspections at this facility

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  • 1107966 (NAI Fri Aug 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1017658 (VAI Fri Feb 24 2017 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))

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