FDA inspection

LifeServe Blood Center: FDA inspection ending May 11, 2012

FDA inspection 781243 · Voluntary Action Indicated (VAI) · Sioux City, IA

Key facts

Inspection ID 781243
Firm LifeServe Blood Center
FEI number 1970344
Address 3300 Line Dr
City Sioux City
State IA
ZIP 51106
Country United States
Fiscal year 2012
Inspection end date May 11, 2012
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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