483 Kulzer. Sep 2011

483 Kulzer. Sep 2011

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FDA investigators audited the Kulzer. - South Bend, IN, United States facility and issued 2 inspectional observations (via FDA 483) on 28 Sep 2011.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 2
  • Inspection end: 28 Sep 2011
  • Location: South Bend, United States
  • FEI: 1821514
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