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FDA Inspection
•Kedplasma LLC•February 3, 2026

Kedplasma LLC – FDA Inspection, Feb 3, 2026

Record Details

This FDA Inspection record concerns Kedplasma LLC, with an inspection on February 3, 2026, issued by the Florida District Office, covering biologics.

Company
Kedplasma LLC
Inspection Date
February 3, 2026
Product Type
Biologics
Office
Florida District Office
People
  • Catherine L. Mcgraw (Issuing Officer)
  • Christi Ann L. Samella (Issuing Officer)
  • Mona B. Amin (Issuing Officer)
View Company Profile

ID · b5cdc60b-1c4b-44ce-a627-b316d763ebfc

Inspection Facts

Inspection number
1314116
FDA center
Biologics
Outcome
Form 483 issued

Other FDA inspections of Kedplasma LLC

6
DateClassificationOfficeProject area
October 18, 2024Not classifiedFlorida District Office
November 1, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 26, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 30, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 18, 2011NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Kedplasma LLC
  • FDA Inspection 1252402 - 2024-10-18
  • FDA Inspection 1073782 - 2018-11-01
  • FDA Inspection 987762 - 2016-08-26
  • FDA Inspection 864145 - 2014-01-30
  • FDA Inspection 753480 - 2011-11-18

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Contact
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