FDA inspection

LifeServe Blood Center: FDA inspection ending Apr 5, 2019

FDA inspection 1088284 · No Action Indicated (NAI) · Sioux City, IA

Key facts

Inspection ID 1088284
Firm LifeServe Blood Center
FEI number 1970344
Address 3300 Line Dr
City Sioux City
State IA
ZIP 51106
Country United States
Fiscal year 2019
Inspection end date Apr 5, 2019
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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