FDA inspection

Electro Kinetic Technologies, LLC: FDA inspection ending Jan 8, 2014

FDA inspection 861890 · No Action Indicated (NAI) · Germantown, WI

Key facts

Inspection ID 861890
Firm Electro Kinetic Technologies, LLC
FEI number 3007903728
Address W194n11301 Mccormick Dr
City Germantown
State WI
ZIP 53022
Country United States
Fiscal year 2014
Inspection end date Jan 8, 2014
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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