FDA issued a Warning Letter to ThyssenKrupp Access Manufacturing, LLC on 3/27/2012 as a result of this inspection.
483 ThyssenKrupp Access Manufacturing Nov 2011

483 ThyssenKrupp Access Manufacturing Nov 2011

Nicole Williams FDA$119.00 - Available Now

FDA investigators audited the ThyssenKrupp Access Manufacturing - Roanoke, IL, United States facility and issued inspectional observations (via FDA 483) on 10 Nov 2011.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 10 Nov 2011
  • Location: Roanoke, United States
  • FEI: 1000139742
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