FDA inspection

Efoora, Inc. dba Virotek, L.L.C.: FDA inspection ending Dec 19, 2003

FDA inspection 304753 · Official Action Indicated (OAI) · Buffalo Grove, IL

Key facts

Inspection ID 304753
Firm Efoora, Inc. dba Virotek, L.L.C.
FEI number 3002689104
Address 900 Asbury Dr
City Buffalo Grove
State IL
ZIP 60089-4557
Fiscal year 2004
Inspection end date Dec 19, 2003
Classification Official Action Indicated (OAI)
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
Warning letter UCM146394

At a glance

  • 10–99 Citations
  • 1–9 Posted citations
  • Yes 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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