FDA issued a Warning Letter to ThyssenKrupp Access Corp. on 8/23/2011 for a previous inspection.
483 ThyssenKrupp Access Apr 2012

483 ThyssenKrupp Access Apr 2012

James Planchon FDA, Cody Rickman FDA$119.00 - Available Now

FDA investigators audited the ThyssenKrupp Access - Grandview, MO, United States facility and issued 5 inspectional observations (via FDA 483) on 10 Apr 2012.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 5
  • Inspection end: 10 Apr 2012
  • Location: Grandview, United States
  • FEI: 1925312
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