Form 483

Richard Wolf Medical Instruments Corp. Form 483, 2009-10-09

FDA issued a Form 483 to Richard Wolf Medical Instruments Corp. on 2009-10-09 with 10 public-safe observations.

483· Form 483 issued10 observations

Richard Wolf Medical Instruments Corp. · Vernon Hills, United States · Issued October 9, 2009

Overview

  • 10 public-safe observations are available for this inspection.
  • 10 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.

9 Oct 2009
21 CFR 820.70(a)

Process control procedures

Cited by Stephen D Eich

9 Oct 2009
21 CFR 820.72(b)(2)

Calibration documentation

Cited by Stephen D Eich

9 Oct 2009
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Stephen D Eich

9 Oct 2009
21 CFR 820.80(a)

Lack of or inadequate procedures - Acceptance activities

Cited by Stephen D Eich

9 Oct 2009
21 CFR 820.90(a)

Nonconforming product control

Cited by Stephen D Eich

Inspected site

RWRichard Wolf Medical Instruments Corp.Vernon Hills, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)(2)Cited across public-safe Form 483 observations1x
21 CFR 820.100(a)(3)Cited across public-safe Form 483 observations1x
21 CFR 820.100(b)Cited across public-safe Form 483 observations1x
21 CFR 820.184(e)Cited across public-safe Form 483 observations1x
21 CFR 820.198(c)Cited across public-safe Form 483 observations1x
21 CFR 820.70(a)Cited across public-safe Form 483 observations1x
21 CFR 820.72(b)(2)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x
21 CFR 820.80(a)Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 10 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