FDA issued a Warning Letter to CryoLife, Inc. on 1/29/2013 as a result of this inspection.
FDA investigators audited the CryoLife - Kennesaw, GA, United States facility and issued inspectional observations (via FDA 483) on 16 Oct 2012.
Product details
- Category: Biologics / Medical Devices & Rad Health
- Inspection end: 16 Oct 2012
- Location: Kennesaw, United States
- FEI: 3001451326
