FDA inspection

EKOS Corporation: FDA inspection ending Sep 26, 2019

FDA inspection 1107256 · No Action Indicated (NAI) · Bothell, WA

Key facts

Inspection ID 1107256
Firm EKOS Corporation
FEI number 3001627457
Address 11911 N Creek Pkwy S
City Bothell
State WA
ZIP 98011
Country United States
Fiscal year 2019
Inspection end date Sep 26, 2019
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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