FDA issued a Warning Letter to CryoLife, Inc. on 1/29/2013 for a later inspection.
483 CryoLife Aug 2005

483 CryoLife Aug 2005

Paul Bonneau FDA, Karen Coleman FDA, Leslie Gilbert FDA, Patricia Hudson FDA, Derek Price FDA, Tammara Stephens FDA, Vincent Williams FDA$119.00 - Available Now

FDA investigators audited the CryoLife - Kennesaw, GA, United States facility and issued inspectional observations (via FDA 483) on 05 Aug 2005.

Product details

  • Category: Biologics / Medical Devices & Rad Health
  • Inspection end: 05 Aug 2005
  • Location: Kennesaw, United States
  • FEI: 3001451326
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