FDA inspection

Laboratoires Delon: FDA inspection ending Dec 9, 2016

FDA inspection 997025 · Voluntary Action Indicated (VAI) · Pointe-Claire

Key facts

Inspection ID 997025
Firm Laboratoires Delon
FEI number 3002698327
Address 75 Hymus Blvd
City Pointe-Claire
Country Canada
Fiscal year 2017
Inspection end date Dec 9, 2016
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

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