FDA inspection

Kedplasma LLC: FDA inspection ending Nov 21, 2016

FDA inspection 994704 · Voluntary Action Indicated (VAI) · Hot Springs, AR

Key facts

Inspection ID 994704
Firm Kedplasma LLC
FEI number 1643463
Address 630 Malvern Ave
City Hot Springs
State AR
ZIP 71901
Country United States
Fiscal year 2017
Inspection end date Nov 21, 2016
Classification Voluntary Action Indicated (VAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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