Form 483

Advantis Medical Form 483, 2018-05-23

FDA issued a Form 483 to Advantis Medical on 2018-05-23 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Advantis Medical · Greenwood, United States · Issued May 23, 2018

Overview

  • 4 public-safe observations are available for this inspection.
  • 2 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.

23 May 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Joseph R Strelnik

23 May 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Joseph R Strelnik

23 May 2018
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Joseph R Strelnik

23 May 2018
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Joseph R Strelnik

Inspected site

AMAdvantis MedicalGreenwood, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.50Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 4 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