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•United States

Kedplasma LLC, Orlando, FL – FDA Inspections

Inspection records and compliance data for Kedplasma LLC in Orlando, Florida. 7 FDA inspections on record, 1 Form 483, last inspected February 03, 2026.

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Company Profile

This profile covers Kedplasma LLC based in Orlando, Florida, United States.

FDA Inspection History

FDA inspections
7
OAI
0
VAI
1
NAI
4
Unclassified
2
Form 483s
1
Warning letters
0

First inspected January 22, 2010. Last inspected February 3, 2026.

Most cited issue areas

  • Donor criteria1 inspection
  • Establish, maintain and follow manufacturing SOPs1 inspection

FDA inspections (7)

DateResultFDA center(s)Insp. #
February 3, 2026Not classifiedBiologics1314116
October 18, 2024Not classifiedBiologics1252402
November 1, 2018NAIBiologics · Blood and Blood Products1073782
August 26, 2016NAIBiologics · Blood and Blood Products987762
January 30, 2014NAIBiologics · Blood and Blood Products864145
November 18, 2011NAIBiologics · Blood and Blood Products753480
January 22, 2010VAIBiologics · Blood and Blood Products639646
FDA documents

Form 483s (1)

  • Form 483s
People (2)
Mona B. Amin
Person
Catherine McDevitt
Person
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Company Information

Name

Kedplasma LLC

FEI Number

3002721889

Address

11601 E Colonial Dr, Orlando, Florida 32817, United States

Country

United States

ID: 73a73078-11e9-4203-b5b6-9ddf25db74a4

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