Form 483

Fresenius Kabi USA LLC Form 483, 2013-12-11

FDA issued a Form 483 to Fresenius Kabi USA LLC on 2013-12-11 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Fresenius Kabi USA LLC · Melrose Park, United States · Issued December 11, 2013

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 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.

11 Dec 2013
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by John M Seale, Russell K Riley

11 Dec 2013
21 CFR 211.63

Equipment Design, Size and Location

Cited by John M Seale, Russell K Riley

11 Dec 2013
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by John M Seale, Russell K Riley

Inspected site

FKFresenius Kabi USA LLCMelrose Park, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.113(b)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x
21 CFR 211.63Cited across public-safe Form 483 observations1x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 3 observations

The source PDF and 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