FDA inspection
LISI MEDICAL FASTENERS: FDA inspection ending Apr 25, 2002
FDA inspection 218994 · Voluntary Action Indicated (VAI) · Miribel Cedex
Key facts
| Inspection ID | 218994 |
|---|---|
| Firm | LISI MEDICAL FASTENERS |
| FEI number | 3003690049 |
| Address | 19 CHEMIN DE LA TRAILLE, Trailleoneyron - Bp 100 |
| City | Miribel Cedex |
| Fiscal year | 2002 |
| Inspection end date | Apr 25, 2002 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
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