FDA inspection

Spentech, Inc.: FDA inspection ending Oct 29, 2003

FDA inspection 300377 · Voluntary Action Indicated (VAI) · Redmond, WA

Key facts

Inspection ID 300377
Firm Spentech, Inc.
FEI number 3003139439
Address 14907 NE 95th St
City Redmond
State WA
ZIP 98052-2559
Fiscal year 2004
Inspection end date Oct 29, 2003
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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