FDA inspection

Hemocue Inc: FDA inspection ending Jan 28, 2004

FDA inspection 310822 · Voluntary Action Indicated (VAI) · Lake Forest, CA

Key facts

Inspection ID 310822
Firm Hemocue Inc
FEI number 2027756
Address 40 Empire Dr
City Lake Forest
State CA
ZIP 92630-2244
Fiscal year 2004
Inspection end date Jan 28, 2004
Classification Voluntary Action Indicated (VAI)
Project area Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices
Product type Biologics, Devices

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
  • 1–9 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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