FDA inspection
Temec Instruments B.V.: FDA inspection ending Nov 24, 2011
FDA inspection 755350 · Voluntary Action Indicated (VAI) · Kerkrade
Key facts
| Inspection ID | 755350 |
|---|---|
| Firm | Temec Instruments B.V. |
| FEI number | 1000634303 |
| Address | Spekhofstraat 2 |
| City | Kerkrade |
| Country | Netherlands |
| Fiscal year | 2012 |
| Inspection end date | Nov 24, 2011 |
| 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
- 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