FDA-Inspected Site

KEDPLASMA LLC

2 FDA inspections are on record for KEDPLASMA LLC in Sanford, United States.

483· Form 483 issued

Sanford, United States · Last updated July 11, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2023-06-26.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
22 Jun 2023 – 26 Jun 2023Biologics483View 483 →
3 Mar 2020 – 5 Mar 2020BiologicsClean

Observations on record

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

26 Jun 2023
21 CFR 640.65(b)(2)(i)

Physician review of four month sample

Cited by Barbara T Carmichael, Lura D Baquero, Lura D Kelly

Investigators

FDA investigators tied to this site in the record.

Lura D Kelly1 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 640.65(b)(2)(i)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind KEDPLASMA LLC'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