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FDA Inspection
•Kedplasma LLC•March 3, 2026

Kedplasma LLC – FDA Inspection, Mar 3, 2026

Record Details

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

Company
Kedplasma LLC
Inspection Date
March 3, 2026
Product Type
Biologics
Office
Dallas District Office
Person
  • Elyshia Q. Danaher (Issuing Officer)
View Company Profile

ID · d213196a-cfcb-4f24-999a-1f5b73622c88

Inspection Facts

Inspection number
1305346
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Kedplasma LLC

1
DateClassificationOfficeProject area
June 6, 2019Not classifiedDallas District Office
Other documents for Kedplasma LLC
  • FDA Inspection 1096378 - 2019-06-06

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