Form 483

Aaren Scientific Inc. Form 483, 2016-05-10

FDA issued a Form 483 to Aaren Scientific Inc. on 2016-05-10 with 15 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health15 observations

Aaren Scientific Inc. · Ontario, United States · Issued May 10, 2016

Overview

  • 15 public-safe observations are available for this inspection.
  • 5 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 May 2016
21 CFR 803.17(a)(2)

Lack of System for Determining MDR Events

Cited by Sonya L Karsik

10 May 2016
21 CFR 803.17(a)(2)

Lack of System for Determining MDR Events

Cited by Sonya L Karsik

10 May 2016
21 CFR 803.17(a)(2)

Lack of System for Determining MDR Events

Cited by Sonya L Karsik

10 May 2016
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Sonya L Karsik

10 May 2016
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Sonya L Karsik

Inspected site

ASAaren Scientific Inc.Ontario, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17(a)(2)Cited across public-safe Form 483 observations3x
21 CFR 803.50(a)(1)Cited across public-safe Form 483 observations3x
21 CFR 803.56Cited across public-safe Form 483 observations3x
21 CFR 820.120Cited across public-safe Form 483 observations3x
21 CFR 820.70(g)Cited across public-safe Form 483 observations3x

Full 483 report

Get the verbatim text of all 15 observations

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