FDA inspection

GluStitch Inc.: FDA inspection ending May 13, 2010

FDA inspection 663259 · Voluntary Action Indicated (VAI) · Delta

Key facts

Inspection ID 663259
Firm GluStitch Inc.
FEI number 3003769089
Address 307-7188 Progress Way
City Delta
Country Canada
Fiscal year 2010
Inspection end date May 13, 2010
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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

Browse all FDA inspections