Form 483

Areva Pharmaceuticals Inc Form 483, 2025-09-11

FDA issued a Form 483 to Areva Pharmaceuticals Inc on 2025-09-11 with 3 public-safe observations.

483· Form 483 issuedHuman Drugs3 observations

Areva Pharmaceuticals Inc · Georgetown, United States · Issued September 11, 2025

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.

11 Sep 2025
21 CFR 314.80(b)

Failure to develop written procedures

Cited by Iris C Macinnes

11 Sep 2025
21 CFR 314.80(c)(2)

Late submission of annual safety reports

Cited by Iris C Macinnes

11 Sep 2025
21 CFR 314.81(b)(2)

Timely submission

Cited by Iris C Macinnes

Inspected site

APAreva Pharmaceuticals IncGeorgetown, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 314.80(b)Cited across public-safe Form 483 observations1x
21 CFR 314.80(c)(2)Cited across public-safe Form 483 observations1x
21 CFR 314.81(b)(2)Cited across public-safe Form 483 observations1x

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 3 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