FDA inspection
Intertek (Schweiz) AG: FDA inspection ending Nov 9, 2016
FDA inspection 992921 · Reinach Bl
Key facts
| Inspection ID | 992921 |
|---|---|
| Firm | Intertek (Schweiz) AG |
| FEI number | 3009832469 |
| Address | Techcenter Reinach, Kagenstrasse 18 |
| City | Reinach Bl |
| Fiscal year | 2017 |
| Inspection end date | Nov 9, 2016 |
| Project area | New Drug Evaluation |
| Product type | Drugs |
At a glance
- None 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