FDA-Inspected Site

Sonivate Medical, Inc.

2 FDA inspections are on record for Sonivate Medical, Inc. in Portland, United States.

483· Form 483 issued

Portland, United States · Last updated July 10, 2026

Overview

  • 2 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2017-05-17.

At a glance

Inspections

2

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
15 May 2017 – 17 May 2017Medical Devices & Rad Health483On file
16 Jan 2014 – 23 Jan 2014Medical Devices & Rad Health483View 483 →

Observations on record

Form 483 observations cited at this site, most recent first.

23 Jan 2014
21 CFR 820.22

Quality audits - auditor independence

Cited by James D Hildreth, Gloria J Baca

23 Jan 2014
21 CFR 820.30(f)

Design verification - output does not meet input requirement

Cited by James D Hildreth, Gloria J Baca

23 Jan 2014
21 CFR 820.80(b)

Lack of or inadequate receiving acceptance procedures

Cited by James D Hildreth, Gloria J Baca

23 Jan 2014
21 CFR 820.90(a)

Nonconforming product, Lack of or inadequate procedures

Cited by James D Hildreth, Gloria J Baca

23 Jan 2014
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by James D Hildreth, Gloria J Baca

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.30(f)Cited across public-safe Form 483 observations1x
21 CFR 820.80(b)Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Sonivate Medical, Inc.'s 2 Form 483s

Verbatim observations and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat