FDA inspection

Sonivate Medical, Inc.: FDA inspection ending May 17, 2017

FDA inspection 1011992 · Voluntary Action Indicated (VAI) · Portland, OR

Key facts

Inspection ID 1011992
Firm Sonivate Medical, Inc.
FEI number 3009565060
Address 4640 SW Macadam Ave
City Portland
State OR
ZIP 97239
Country United States
Fiscal year 2017
Inspection end date May 17, 2017
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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