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FDA Inspection 1055914 — Bayer OY

Bayer OY — FEI 1000350927

The FDA completed an inspection of Bayer OY on June 1, 2018 in Turku. 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
June 1, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Turku (Finland)

Facility

Other inspections at this facility

  • 1273226 (VAI Fri Sep 15 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 972548 (VAI Fri Apr 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 803182 (NAI Tue Oct 02 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 762223 (NAI Thu Dec 15 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 694779 (NAI Fri Sep 24 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources