Form 483

Medline Industries, LP Form 483, 2008-12-11

FDA issued a Form 483 to Medline Industries, LP on 2008-12-11 with 5 public-safe observations.

483· Form 483 issued5 observations

Medline Industries, LP · Northfield, United States · Issued December 11, 2008

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 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.

11 Dec 2008
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Stephen D Eich

11 Dec 2008
21 CFR 820.50(a)

Evaluation of suppliers, contractors, etc., requirements

Cited by Stephen D Eich

11 Dec 2008
21 CFR 820.70(a)

Production processes

Cited by Stephen D Eich

11 Dec 2008
21 CFR 820.100(a)(1)

Analysis of data sources

Cited by Stephen D Eich

11 Dec 2008
21 CFR 820.100(a)(2)

Investigation

Cited by Stephen D Eich

Inspected site

MIMedline Industries, LPNorthfield, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)(1)Cited across public-safe Form 483 observations1x
21 CFR 820.100(a)(2)Cited across public-safe Form 483 observations1x
21 CFR 820.50Cited across public-safe Form 483 observations1x
21 CFR 820.50(a)Cited across public-safe Form 483 observations1x
21 CFR 820.70(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 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