FDA-Inspected Site

Ekso Bionics

3 FDA inspections are on record for Ekso Bionics in Richmond, United States.

Clean· No action indicated

Richmond, United States · Last updated July 10, 2026

Overview

  • 3 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2025-05-20.

At a glance

Inspections

3

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
20 May 2025Medical Devices & Rad HealthClean
28 Jun 2019Medical Devices & Rad HealthClean
2 Sep 2015 – 11 Sep 2015Medical Devices & Rad Health483View 483 →

Observations on record

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

11 Sep 2015
21 CFR 50.25(a)(4)

Alternate procedures, courses of treatment

Cited by Jane M Kreis

11 Sep 2015
21 CFR 50.25(c)

ClincialTrials.gov statement

Cited by Jane M Kreis

11 Sep 2015
21 CFR 812.140(b)(6)

Other sponsor records required by FDA inadequate

Cited by Jane M Kreis

11 Sep 2015
21 CFR 812.150(b)(1)

Sponsor evaluation rpt not timely, distributed

Cited by Jane M Kreis

Investigators

FDA investigators tied to this site in the record.

State Agency1 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 50.25(a)(4)Cited across public-safe Form 483 observations1x
21 CFR 50.25(c)Cited across public-safe Form 483 observations1x
21 CFR 812.140(b)(6)Cited across public-safe Form 483 observations1x
21 CFR 812.150(b)(1)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Ekso Bionics' 1 Form 483

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