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FDA Inspection 843541 — ThyssenKrupp Access Corp

ThyssenKrupp Access Corp — FEI 1925312

The FDA completed an inspection of ThyssenKrupp Access Corp on August 8, 2013 in Grandview, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 8, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Grandview, MO (United States)

Facility

Other inspections at this facility

  • 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))
  • 601903 (VAI Wed Aug 05 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources