Form 483

Genesis BPS, LLC. Form 483, 2017-11-20

FDA issued a Form 483 to Genesis BPS, LLC. on 2017-11-20 with 8 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health8 observations

Genesis BPS, LLC. · Ramsey, United States · Issued November 20, 2017

Overview

  • 8 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

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

20 Nov 2017
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Melissa A Freeman, Melissa A Zuppe

20 Nov 2017
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Melissa A Freeman, Melissa A Zuppe

20 Nov 2017
21 CFR 820.198(a)

Complaints

Cited by Melissa A Freeman, Melissa A Zuppe

20 Nov 2017
21 CFR 820.198(a)

Complaints

Cited by Melissa A Freeman, Melissa A Zuppe

20 Nov 2017
21 CFR 820.30(g)

Design validation - production units

Cited by Melissa A Freeman, Melissa A Zuppe

Inspected site

GBGenesis BPS, LLC.Ramsey, 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
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.30(g)Cited across public-safe Form 483 observations2x
21 CFR 820.40(a)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 and 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