Form 483

Ekso Bionics Form 483, 2015-09-11

FDA issued a Form 483 to Ekso Bionics on 2015-09-11 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Ekso Bionics · Richmond, United States · Issued September 11, 2015

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

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

Inspected site

EBEkso BionicsRichmond, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

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 483 report

Get the verbatim text of all 4 observations

Every observation in full, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere