FDA inspection
Ropack, Inc. (Site A & B): FDA inspection ending Jan 21, 2016
FDA inspection 957414 · Official Action Indicated (OAI) · Anjou
Key facts
| Inspection ID | 957414 |
|---|---|
| Firm | Ropack, Inc. (Site A & B) |
| FEI number | 3002674295 |
| Address | 10801 Mirabeau St |
| City | Anjou |
| Country | Canada |
| Fiscal year | 2016 |
| Inspection end date | Jan 21, 2016 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 499580 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes 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