Form 483

Akers Biosciences, Inc. Form 483, 2012-04-11

FDA issued a Form 483 to Akers Biosciences, Inc. on 2012-04-11 with 4 public-safe observations.

483· Form 483 issued4 observations

Akers Biosciences, Inc. · Thorofare, United States · Issued April 11, 2012

Overview

  • 4 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.

11 Apr 2012
21 CFR 820.20(c)

Management review - Lack of or inadequate procedures

Cited by Loretta Nemchik

11 Apr 2012
21 CFR 820.22

Quality audits - Lack of or inadequate procedures

Cited by Loretta Nemchik

11 Apr 2012
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Loretta Nemchik

11 Apr 2012
21 CFR 820.80(a)

Lack of or inadequate procedures - Acceptance activities

Cited by Loretta Nemchik

Inspected site

ABAkers Biosciences, Inc.Thorofare, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.20(c)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x
21 CFR 820.80(a)Cited across public-safe Form 483 observations1x

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 4 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