Form 483

VectraCor, Inc Form 483, 2017-09-27

FDA issued a Form 483 to VectraCor, Inc on 2017-09-27 with 2 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health2 observations

VectraCor, Inc · Totowa, United States · Issued September 27, 2017

Overview

  • 2 public-safe observations are available for this inspection.
  • 1 structured CFR citation is represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

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

27 Sep 2017
21 CFR 820.198(e)

Records of complaint investigation

Cited by Melissa A Freeman, Melissa A Zuppe

27 Sep 2017
21 CFR 820.198(e)

Records of complaint investigation

Cited by Melissa A Freeman, Melissa A Zuppe

Inspected site

VIVectraCor, IncTotowa, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(e)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 2 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