Form 483

Octapharma Plasma Inc. Form 483, 2025-06-05

FDA issued a Form 483 to Octapharma Plasma Inc. on 2025-06-05 with 2 public-safe observations.

483· Form 483 issuedBiologics2 observations

Octapharma Plasma Inc. · Sparks, United States · Issued June 5, 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.

5 Jun 2025
21 CFR 606.100(b)(2)

Donor qualifying tests & measurements

Cited by Shelley H Beausoleil

5 Jun 2025
21 CFR 630.10(a)

Donor Eligibility Factors

Cited by Shelley H Beausoleil

Inspected site

OPOctapharma Plasma Inc.Sparks, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 606.100(b)(2)Cited across public-safe Form 483 observations1x
21 CFR 630.10(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

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