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483 Electro Kinetic Technologies, Feb 2019

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FDA investigators audited the Electro Kinetic Technologies - Germantown , WI, United States facility and issued inspectional observations (via FDA 483) on 15 Feb 2019.

Product Details

  • Category: Medical Devices & Rad Health
  • Inspection end: 15 Feb 2019
  • Location: Germantown, United States
  • FEI: 3007903728
Electro Kinetic Technologies FDA inspection 483 Feb 2019

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483 Electro Kinetic Technologies Germantown Jan 2013 product image

483 Electro Kinetic Technologies Germantown Jan 2013

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Issued: 17 Jan 2013