FDA-Inspected Site

Kedplasma LLC

9 FDA inspections are on record for Kedplasma LLC in Orlando, United States.

483· Form 483 issued

Orlando, United States · Last updated July 10, 2026

Overview

  • 9 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2026-02-03.

At a glance

Inspections

9

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
2 Feb 2026 – 3 Feb 2026Biologics483On file
16 Oct 2024 – 18 Oct 2024BiologicsClean
31 Oct 2018 – 1 Nov 2018BiologicsClean
22 Aug 2016 – 26 Aug 2016BiologicsClean
29 Jan 2014 – 30 Jan 2014BiologicsClean
18 Nov 2011Not recordedClean
22 Jan 2010Not recorded483View 483 →
11 Jan 2008Not recordedClean
21 Nov 2000Not recordedClean

Observations on record

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

22 Jan 2010
21 CFR 606.100(b)

Establish, maintain and follow manufacturing SOPs

Cited by Jana L Caylor, Ronnie E Jackson

22 Jan 2010
21 CFR 606.100(b)(1)

Donor criteria

Cited by Jana L Caylor, Ronnie E Jackson

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 606.100(b)(1)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Kedplasma LLC's 2 Form 483s

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