Form 483

SPARROW ROBOT, LLC Form 483, 2026-04-10

FDA issued a Form 483 to SPARROW ROBOT, LLC on 2026-04-10 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

SPARROW ROBOT, LLC · Columbus, United States · Issued April 10, 2026

Overview

  • 6 public-safe observations are available for this inspection.
  • 3 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.

10 Apr 2026
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Javonica F Penn

10 Apr 2026
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Javonica F Penn

10 Apr 2026
ISO 13485:2016 Clause 4.1.1

QMS not documented and maintained adequately

Cited by Javonica F Penn

10 Apr 2026
ISO 13485:2016 Clause 4.1.1

QMS not documented and maintained adequately

Cited by Javonica F Penn

10 Apr 2026
ISO 13485:2016 Clause 7.1

Processes needed for product realization not planned and developed

Cited by Javonica F Penn

Inspected site

SRSPARROW ROBOT, LLCColumbus, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17Cited across public-safe Form 483 observations2x
ISO 13485:2016 Clause 4.1.1Cited across public-safe Form 483 observations2x
ISO 13485:2016 Clause 7.1Cited across public-safe Form 483 observations2x

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