Form 483

Trireme Medical, Inc. Form 483, 2019-10-30

FDA issued a Form 483 to Trireme Medical, Inc. on 2019-10-30 with 8 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health8 observations

Trireme Medical, Inc. · Pleasanton, United States · Issued October 30, 2019

Overview

  • 8 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.

30 Oct 2019
21 CFR 812.140(b)(3)

Sponsor records of investigator agreements inadequate

Cited by Kristin M Abaonza

30 Oct 2019
21 CFR 812.40

Sponsors' general responsibilities

Cited by Kristin M Abaonza

30 Oct 2019
21 CFR 812.43(c)

No investigator agreement

Cited by Kristin M Abaonza

30 Oct 2019
21 CFR 812.43(c)(5)

No financial disclosure info in investigator agreement

Cited by Kristin M Abaonza

30 Oct 2019
21 CFR 812.140(b)(3)

Sponsor records of investigator agreements inadequate

Cited by Kristin M Abaonza

Inspected site

TMTrireme Medical, Inc.Pleasanton, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 812.140(b)(3)Cited across public-safe Form 483 observations2x
21 CFR 812.40Cited across public-safe Form 483 observations2x
21 CFR 812.43(c)Cited across public-safe Form 483 observations2x
21 CFR 812.43(c)(5)Cited across public-safe Form 483 observations2x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 8 observations

The source PDF, 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