Form 483

Hans Rudolph Inc Form 483, 2017-02-22

FDA issued a Form 483 to Hans Rudolph Inc on 2017-02-22 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Hans Rudolph Inc · Shawnee, United States · Issued February 22, 2017

Overview

  • 4 public-safe observations are available for this inspection.
  • 2 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.

22 Feb 2017
21 CFR 820.198(e)

Records of complaint investigation

Cited by Eric C Fox

22 Feb 2017
21 CFR 820.198(e)

Records of complaint investigation

Cited by Eric C Fox

22 Feb 2017
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Eric C Fox

22 Feb 2017
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Eric C Fox

Inspected site

HRHans Rudolph IncShawnee, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(e)Cited across public-safe Form 483 observations2x
21 CFR 820.75(a)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 4 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