Home / Inspections / 601903

FDA Inspection 601903 — ThyssenKrupp Access Corp

ThyssenKrupp Access Corp — FEI 1925312

The FDA completed an inspection of ThyssenKrupp Access Corp on August 5, 2009 in Grandview, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 5, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Grandview, MO (United States)

Facility

Other inspections at this facility

  • 843541 (NAI Thu Aug 08 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 777303 (VAI Tue Apr 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 714462 (OAI Thu Mar 10 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources