483
Kedplasma LLCKedplasma LLC – FDA 483
Record Details
KEDPLASMA LLC in Orlando, FL, was issued a Form 483 following an inspection from February 2-3, 2026. The inspection identified a failure to adhere to established procedures designed to ensure donor safety and program compliance. Specifically, a donor in an immunization program did not receive required physical examinations, even when a system prompt indicated the exam was overdue.
- Company
- Kedplasma LLC
- Product type
- biologics
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ID · 13969a6b-c08d-4338-a6fb-e59e3f6b0e5e
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