FDA inspection

Ropack, Inc. (Site A & B): FDA inspection ending Oct 21, 2008

FDA inspection 545831 · Voluntary Action Indicated (VAI) · Anjou

Key facts

Inspection ID 545831
Firm Ropack, Inc. (Site A & B)
FEI number 3002674295
Address 10801 Mirabeau St
City Anjou
Country Canada
Fiscal year 2009
Inspection end date Oct 21, 2008
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
  • 10–99 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