Form 483

DASISIMULATIONS, LLC Form 483, 2026-01-16

FDA issued a Form 483 to DASISIMULATIONS, LLC on 2026-01-16 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

DASISIMULATIONS, LLC · Dublin, United States · Issued January 16, 2026

Overview

  • 6 public-safe observations are available for this inspection.
  • 6 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.

16 Jan 2026
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Rosanna M Goodrich

16 Jan 2026
21 CFR 820.22

Quality audits - Lack of or inadequate procedures

Cited by Rosanna M Goodrich

16 Jan 2026
21 CFR 820.25(b)

Training - Lack of or inadequate procedures

Cited by Rosanna M Goodrich

16 Jan 2026
21 CFR 820.30(g)

Design Validation - Risk analysis not performed/inadequate

Cited by Rosanna M Goodrich

16 Jan 2026
21 CFR 820.40

Procedures not adequately established or maintained

Cited by Rosanna M Goodrich

Inspected site

DLDASISIMULATIONS, LLCDublin, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

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 820.25(b)Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x
21 CFR 820.40Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 6 observations

The full inspection record, as Atlas holds it, 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