Atlas

FDA-Inspected Site

OneBlood, Inc.

8 FDA inspections are on record for OneBlood, Inc. in Rockledge, United States.

483· Form 483 issued

Rockledge, United States · Last updated August 15, 2026

Overview

  • 8 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2026-03-26.

At a glance

Inspections

8

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
24 Mar 2026 – 26 Mar 2026Biologics483View 483 →
5 Feb 2020 – 6 Feb 2020BiologicsClean
14 Nov 2017BiologicsClean
2 Aug 2016BiologicsClean
26 Aug 2014BiologicsClean
16 Nov 2012Not recordedClean
8 Nov 2010Not recordedClean
12 Nov 2008Not recordedClean

Observations on record

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

26 Mar 2026
21 CFR 606.171

Biological product deviation report

Cited by Mizanne E Lewis

Investigators

FDA investigators tied to this site in the record.

Mizanne E Lewis3 insp.
Lura D Baquero1 insp.
Ashley B Jelonek1 insp.
Stacey F Allard1 insp.
Angela E Glenn1 insp.
Jana L Caylor1 insp.
Ronnie E Jackson1 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 606.171Cited across public-safe Form 483 observations1x

Full site report

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

Source PDFs 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