Form 483

Dendreon Pharmaceuticals LLC Form 483, 2025-10-29

FDA issued a Form 483 to Dendreon Pharmaceuticals LLC on 2025-10-29 with 2 public-safe observations.

483· Form 483 issuedBiologics2 observations

Dendreon Pharmaceuticals LLC · Union City, United States · Issued October 29, 2025

Overview

  • 2 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.

29 Oct 2025
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Brentley S Pittman

29 Oct 2025
21 CFR 211.194(a)

Complete test data included in records

Cited by Brentley S Pittman

Inspected site

DPDendreon Pharmaceuticals LLCUnion City, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.110(a)Cited across public-safe Form 483 observations1x
21 CFR 211.194(a)Cited across public-safe Form 483 observations1x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 2 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