FDA issued a Warning Letter to Sorin Group Deutschland GmbH on 12/29/2015 for a later inspection.
483 Sorin Group USA Jul 2008

483 Sorin Group USA Jul 2008

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FDA investigators audited the Sorin Group USA - Arvada, CO, United States facility and issued inspectional observations (via FDA 483) on 25 Jul 2008.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 25 Jul 2008
  • Location: Arvada, United States
  • FEI: 1718850
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