Form 483

Eurofins Donor & Product Testing, LLC, San Ramon Form 483, 2025-07-18

FDA issued a Form 483 to Eurofins Donor & Product Testing, LLC, San Ramon on 2025-07-18 with 4 public-safe observations.

483· Form 483 issuedBiologics4 observations

Eurofins Donor & Product Testing, LLC, San Ramon · San Ramon, United States · Issued July 18, 2025

Overview

  • 4 public-safe observations are available for this inspection.
  • 3 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

18 Jul 2025
21 CFR 1271.270(a)

Accurate, indelible, legible

Cited by William F Lagud, Lesley Mae P Lutao

18 Jul 2025
21 CFR 1271.270(a)

Records incomplete

Cited by William F Lagud, Lesley Mae P Lutao

18 Jul 2025
21 CFR 1271.270(d)

Retention time (10 year rules)

Cited by William F Lagud, Lesley Mae P Lutao

18 Jul 2025
21 CFR 1271.80(c)

Manufacturer instructions not followed

Cited by William F Lagud, Lesley Mae P Lutao

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 1271.270(a)Cited across public-safe Form 483 observations2x
21 CFR 1271.270(d)Cited across public-safe Form 483 observations1x
21 CFR 1271.80(c)Cited across public-safe Form 483 observations1x

Source document

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PDF available

Form 483 source document

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Full 483 report

Get the verbatim text of all 4 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