FDA inspection
Peter Lazic (manufacturing site): FDA inspection ending Oct 2, 2002
FDA inspection 240668 · No Action Indicated (NAI) · Tuttlingen
Key facts
| Inspection ID | 240668 |
|---|---|
| Firm | Peter Lazic (manufacturing site) |
| FEI number | 3719 |
| Address | 39 Dornierstrabe |
| City | Tuttlingen |
| Fiscal year | 2003 |
| Inspection end date | Oct 2, 2002 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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