FDA-Inspected Site

Octapharma Plasma Inc

2 FDA inspections are on record for Octapharma Plasma Inc in Mesa, United States.

483· Form 483 issued

Mesa, United States · Last updated July 11, 2026

Overview

  • 2 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2026-05-14.

At a glance

Inspections

2

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
11 May 2026 – 14 May 2026Biologics483View 483 →
14 Jan 2020 – 16 Jan 2020Biologics483On file

Observations on record

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

14 May 2026
21 CFR 606.60(b)

Equipment calibration frequency

Cited by Garrad R Poole

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 606.60(b)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Octapharma Plasma Inc's 2 Form 483s

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