FDA issued a Warning Letter to Sorin Group Deutschland GmbH on 8/2/2011 as a result of this inspection.
483 Sorin Group Deutschland Apr 2011

483 Sorin Group Deutschland Apr 2011

Maribeth Niesen FDA$119.00 - Available Now

FDA investigators audited the Sorin Group Deutschland - Munich, Germany facility and issued inspectional observations (via FDA 483) on 13 Apr 2011.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 13 Apr 2011
  • Location: Munich, Germany
  • FEI: 3002808267
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