483 CDB Sep 2019

483 CDB Sep 2019

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FDA investigators audited the CDB - Leland, NC, United States facility and issued inspectional observations (via FDA 483) on 12 Sep 2019.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 12 Sep 2019
  • Location: Leland, United States
  • FEI: 3003069616
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