Form 483

Arciplex Llc Form 483, 2016-06-28

FDA issued a Form 483 to Arciplex Llc on 2016-06-28 with 7 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health7 observations

Arciplex Llc · Nashville, United States · Issued June 28, 2016

Overview

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

Inspectional observations

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

28 Jun 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Bonnie E Conley, Bonnie E Pierson

28 Jun 2016
21 CFR 820.184

DHR content

Cited by Bonnie E Conley, Bonnie E Pierson

28 Jun 2016
21 CFR 820.20(c)

Management review - defined interval, sufficient frequency

Cited by Bonnie E Conley, Bonnie E Pierson

28 Jun 2016
21 CFR 820.22

Quality audits - Lack of or inadequate procedures

Cited by Bonnie E Conley, Bonnie E Pierson

28 Jun 2016
21 CFR 820.25(b)

Training records

Cited by Bonnie E Conley, Bonnie E Pierson

Inspected site

ALArciplex LlcNashville, 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 observations1x
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.20(c)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.25(b)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x
21 CFR 820.80(e)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 7 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