Form 483

Geneva Laboratories, Inc Form 483, 2018-04-05

FDA issued a Form 483 to Geneva Laboratories, Inc on 2018-04-05 with 8 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health8 observations

Geneva Laboratories, Inc · Elkhorn, United States · Issued April 5, 2018

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.

5 Apr 2018
21 CFR 58.29(a)

Personnel: education, training, experience

Cited by Denise L Burosh

5 Apr 2018
21 CFR 58.35(a)

QAU: separate and independent

Cited by Denise L Burosh

5 Apr 2018
21 CFR 58.35(b)(3)

QAU: inspect study at adequate intervals

Cited by Denise L Burosh

5 Apr 2018
21 CFR 58.63(a)

Equipment: calibration

Cited by Denise L Burosh

5 Apr 2018
21 CFR 58.29(a)

Personnel: education, training, experience

Cited by Denise L Burosh

Inspected site

GLGeneva Laboratories, IncElkhorn, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 58.29(a)Cited across public-safe Form 483 observations2x
21 CFR 58.35(a)Cited across public-safe Form 483 observations2x
21 CFR 58.35(b)(3)Cited across public-safe Form 483 observations2x
21 CFR 58.63(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, 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