FDA issued a Warning Letter to Terumo Cardiovascular Systems on 8/31/2006 for a previous inspection.
483 Terumo Cardiovascular Systems Mar 2010

483 Terumo Cardiovascular Systems Mar 2010

Ryan Benedict FDA, Kimberly Lewandowski-Walker FDA, Charles Spyr FDA, Gary Urbiel Goldner FDA$119.00 - Available Now

FDA investigators audited the Terumo Cardiovascular Systems - Ann Arbor, MI, United States facility and issued 15 inspectional observations (via FDA 483) on 29 Mar 2010.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 15
  • Inspection end: 29 Mar 2010
  • Location: Ann Arbor, United States
  • FEI: 1828100
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