FDA inspection

MicroVision, Inc.: FDA inspection ending Jun 10, 2003

FDA inspection 280338 · Voluntary Action Indicated (VAI) · Seabrook, NH

Key facts

Inspection ID 280338
Firm MicroVision, Inc.
FEI number 3002532015
Address 20 London Ln
City Seabrook
State NH
ZIP 03874-4328
Fiscal year 2003
Inspection end date Jun 10, 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
  • 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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