FDA inspection

Coroneo Inc: FDA inspection ending Mar 9, 2018

FDA inspection 1079284 · Voluntary Action Indicated (VAI) · Montreal

Key facts

Inspection ID 1079284
Firm Coroneo Inc
FEI number 3003320928
Address 9250 Du Parc Ave
City Montreal
Fiscal year 2018
Inspection end date Mar 9, 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

Browse all FDA inspections