FDA issued a Warning Letter to Terumo Cardiovascular Systems on 8/31/2006 as a result of this inspection.
483 Terumo Cardiovascular Systems Dec 2005

483 Terumo Cardiovascular Systems Dec 2005

Benjamin Smith FDA, William Tingley FDA$119.00 - Available Now

FDA investigators audited the Terumo Cardiovascular Systems - Ann Arbor, MI, United States facility and issued 3 inspectional observations (via FDA 483) on 09 Dec 2005.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 3
  • Inspection end: 09 Dec 2005
  • Location: Ann Arbor, United States
  • FEI: 1828100
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