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

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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