Form 483

CareFusion 213, LLC Form 483, 2015-06-25

FDA issued a Form 483 to CareFusion 213, LLC on 2015-06-25 with 12 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health12 observations

CareFusion 213, LLC · El Paso, United States · Issued June 25, 2015

Overview

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

25 Jun 2015
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Arie Menachem, Paul A Bonneau

25 Jun 2015
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Arie Menachem, Paul A Bonneau

25 Jun 2015
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Arie Menachem, Paul A Bonneau

25 Jun 2015
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Arie Menachem, Paul A Bonneau

25 Jun 2015
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Arie Menachem, Paul A Bonneau

Inspected site

C2CareFusion 213, LLCEl Paso, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.113(a)Cited across public-safe Form 483 observations3x
21 CFR 211.192Cited across public-safe Form 483 observations3x
21 CFR 211.46(b)Cited across public-safe Form 483 observations3x
21 CFR 211.84(d)(1)Cited across public-safe Form 483 observations3x

Source document

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PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 12 observations

The source PDF, 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