483 IanTech Sep 2017

483 IanTech Sep 2017

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FDA investigators audited the IanTech - Reno, NV, United States facility and issued inspectional observations (via FDA 483) on 15 Sep 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 15 Sep 2017
  • Location: Reno, United States
  • FEI: 3012123033
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