FDA inspection

Kedplasma LLC: FDA inspection ending Dec 11, 2024

FDA inspection 1257069 · No Action Indicated (NAI) · Greenville, NC

Key facts

Inspection ID 1257069
Firm Kedplasma LLC
FEI number 3003645334
Address 2727 E 10th St
City Greenville
State NC
ZIP 27858
Country United States
Fiscal year 2025
Inspection end date Dec 11, 2024
Classification No Action Indicated (NAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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