FDA issued a Warning Letter to Sorin Group Deutschland GmbH on 12/29/2015 for a later inspection.
483 Sorin Group USA Mar 2013

483 Sorin Group USA Mar 2013

Janet Pulver FDA, Amanda Zorn FDA$119.00 - Available Now

FDA investigators audited the Sorin Group USA - Arvada, CO, United States facility and issued 2 inspectional observations (via FDA 483) on 26 Mar 2013.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 2
  • Inspection end: 26 Mar 2013
  • Location: Arvada, United States
  • FEI: 1718850
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