FDA inspection

Rehabtronics Inc.: FDA inspection ending Sep 28, 2018

FDA inspection 1121814 · Voluntary Action Indicated (VAI) · Edmonton

Key facts

Inspection ID 1121814
Firm Rehabtronics Inc.
FEI number 3007999109
Address 4352-10230 Jasper Ave Nw
City Edmonton
Fiscal year 2018
Inspection end date Sep 28, 2018
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical 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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