FDA-Inspected Site

SI-BONE, Inc.

4 FDA inspections are on record for SI-BONE, Inc. in Santa Clara, United States.

Clean· No action indicated

Santa Clara, United States · Last updated August 15, 2026

Overview

  • 4 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2022-03-31.

At a glance

Inspections

4

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
16 Mar 2022 – 31 Mar 2022Medical Devices & Rad HealthClean
16 Mar 2022 – 22 Mar 2022Medical Devices & Rad HealthClean
29 Nov 2016 – 6 Dec 2016Medical Devices & Rad HealthClean
7 May 2014 – 20 May 2014Medical Devices & Rad Health483View 483 →

Observations on record

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

20 May 2014
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Linda Linh T Nguyen

20 May 2014
21 CFR 820.30(g)

Design validation - user needs and intended uses

Cited by Linda Linh T Nguyen

20 May 2014
21 CFR 820.184

Lack of or inadequate DHR procedures

Cited by Linda Linh T Nguyen

Investigators

FDA investigators tied to this site in the record.

CntrctMntr KingJ1 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 803.17Cited across public-safe Form 483 observations1x
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind SI-BONE, Inc.'s 1 Form 483

Source PDFs, 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