Form 483

Delcath Systems Inc. Form 483, 2023-06-09

FDA issued a Form 483 to Delcath Systems Inc. on 2023-06-09 with 9 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health9 observations

Delcath Systems Inc. · Queensbury, United States · Issued June 9, 2023

Overview

  • 9 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.

9 Jun 2023
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Jacqueline S Warner

9 Jun 2023
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Jacqueline S Warner

9 Jun 2023
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Jacqueline S Warner

9 Jun 2023
21 CFR 820.100(b)

Documentation

Cited by Jacqueline S Warner

9 Jun 2023
21 CFR 820.100(b)

Documentation

Cited by Jacqueline S Warner

Inspected site

DSDelcath Systems Inc.Queensbury, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.50(a)(1)Cited across public-safe Form 483 observations3x
21 CFR 820.100(b)Cited across public-safe Form 483 observations3x
21 CFR 820.50(b)Cited across public-safe Form 483 observations3x

Source document

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PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 9 observations

The source PDF, 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