FDA inspection
Avery Dennison Belgie BV: FDA inspection ending Apr 23, 2015
FDA inspection 931135 · Voluntary Action Indicated (VAI) · Turnhout
Key facts
| Inspection ID | 931135 |
|---|---|
| Firm | Avery Dennison Belgie BV |
| FEI number | 3005360738 |
| Address | Tieblokkenlaan 1 |
| City | Turnhout |
| Country | Belgium |
| Fiscal year | 2015 |
| Inspection end date | Apr 23, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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