FDA inspection

Covalon Technologies Ltd.: FDA inspection ending Sep 12, 2018

FDA inspection 1132036 · Voluntary Action Indicated (VAI) · Mississauga

Key facts

Inspection ID 1132036
Firm Covalon Technologies Ltd.
FEI number 3005004019
Address 1660 Tech Ave Unit 5
City Mississauga
Fiscal year 2018
Inspection end date Sep 12, 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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