Form 483

Karl Storz Endovision, Inc. Form 483, 2013-08-26

FDA issued a Form 483 to Karl Storz Endovision, Inc. on 2013-08-26 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Karl Storz Endovision, Inc. · Charlton, United States · Issued August 26, 2013

Overview

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

26 Aug 2013
21 CFR 820.70(a)

Process control procedures, Lack of or inadequate procedures

Cited by Camerson E Moore

26 Aug 2013
21 CFR 820.70(g)(1)

Maintenance schedule, Lack of or inadequate schedule

Cited by Camerson E Moore

26 Aug 2013
21 CFR 820.184

DHR content

Cited by Camerson E Moore

Inspected site

KSKarl Storz Endovision, Inc.Charlton, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.70(a)Cited across public-safe Form 483 observations1x
21 CFR 820.70(g)(1)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 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