FDA inspection

Hansamed Ltd.: FDA inspection ending Jan 14, 2016

FDA inspection 958313 · Voluntary Action Indicated (VAI) · Laval

Key facts

Inspection ID 958313
Firm Hansamed Ltd.
FEI number 3004431266
Address 3300 Sud Laval (A-440) W
City Laval
Country Canada
Fiscal year 2016
Inspection end date Jan 14, 2016
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