FDA inspection

STERIS Canada ULC: FDA inspection ending Aug 14, 2014

FDA inspection 895054 · Voluntary Action Indicated (VAI) · Quebec

Key facts

Inspection ID 895054
Firm STERIS Canada ULC
FEI number 3004097451
Address 490 Boulevard Armand-Paris
City Quebec
Country Canada
Fiscal year 2014
Inspection end date Aug 14, 2014
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type 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

Browse all FDA inspections