FDA-Inspected Site

KEDPLASMA, LLC

6 FDA inspections are on record for KEDPLASMA, LLC in Lubbock, United States.

Clean· No action indicated

Lubbock, United States · Last updated July 9, 2026

Overview

  • 6 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2023-03-02.

At a glance

Inspections

6

Form 483s

2

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
27 Feb 2023 – 2 Mar 2023BiologicsClean
15 May 2017 – 17 May 2017BiologicsClean
16 Dec 2014 – 18 Dec 2014BiologicsClean
11 Jun 2013 – 13 Jun 2013Biologics483View 483 →
18 Mar 2011Not recordedClean
20 Mar 2009Not recorded483On file

Observations on record

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

13 Jun 2013
21 CFR 606.100(b)

Establish, maintain and follow manufacturing SOPs

Cited by Young M Yoon

Investigators

FDA investigators tied to this site in the record.

Patricia M Jacobs1 insp.

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

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