Form 483

LifeSource-Upper Midwest OPO Form 483, 2012-01-24

FDA issued a Form 483 to LifeSource-Upper Midwest OPO on 2012-01-24 with 3 public-safe observations.

483· Form 483 issued3 observations

LifeSource-Upper Midwest OPO · Minneapolis, United States · Issued January 24, 2012

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.

24 Jan 2012
21 CFR 1271.160(a)

All core requirements covered in program

Cited by Sandra Sejdinovic, Kellie L Westerbuhr

24 Jan 2012
21 CFR 1271.180(a)

Procedures to meet core CTGP

Cited by Sandra Sejdinovic, Kellie L Westerbuhr

24 Jan 2012
21 CFR 1271.270(a)

Accurate, indelible, legible

Cited by Sandra Sejdinovic, Kellie L Westerbuhr

Inspected site

LMLifeSource-Upper Midwest OPOMinneapolis, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 1271.160(a)Cited across public-safe Form 483 observations1x
21 CFR 1271.180(a)Cited across public-safe Form 483 observations1x
21 CFR 1271.270(a)Cited 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