FDA inspection

One Lambda Inc: FDA inspection ending Sep 14, 2006

FDA inspection 443463 · Voluntary Action Indicated (VAI) · Canoga Park, CA

Key facts

Inspection ID 443463
Firm One Lambda Inc
FEI number 2024375
Address 21001 Kittridge St
City Canoga Park
State CA
ZIP 91303-2801
Fiscal year 2006
Inspection end date Sep 14, 2006
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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