FDA-Inspected Site

Octapharma Plasma, Inc.

3 FDA inspections are on record for Octapharma Plasma, Inc. in Redford, United States.

Clean· No action indicated

Redford, United States · Last updated July 10, 2026

Overview

  • 3 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2023-10-20.

At a glance

Inspections

3

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
17 Oct 2023 – 20 Oct 2023BiologicsClean
17 Oct 2018 – 19 Oct 2018Biologics483View 483 →
14 Jun 2016 – 16 Jun 2016BiologicsClean

Observations on record

Form 483 observations cited at this site, most recent first.

19 Oct 2018
21 CFR 606.100(b)

Establish, maintain and follow manufacturing SOPs

Cited by Susan M North

19 Oct 2018
21 CFR 606.40

Clean & orderly

Cited by Susan M North

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 606.100(b)Cited across public-safe Form 483 observations1x
21 CFR 606.40Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Octapharma Plasma, Inc.'s 1 Form 483

Verbatim observations and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat