FDA inspection

Angiotech Biomaterials Corporation: FDA inspection ending Sep 19, 2005

FDA inspection 395767 · No Action Indicated (NAI) · Palo Alto, CA

Key facts

Inspection ID 395767
Firm Angiotech Biomaterials Corporation
FEI number 3002203503
Address 2500 Faber Pl
City Palo Alto
State CA
ZIP 94303-3329
Fiscal year 2005
Inspection end date Sep 19, 2005
Classification No Action Indicated (NAI)
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

  • None Citations
  • None 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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