FDA inspection
GSI Lumonics Inc: FDA inspection ending Nov 30, 2000
FDA inspection 57583 · Oxnard, CA
Key facts
| Inspection ID | 57583 |
|---|---|
| Firm | GSI Lumonics Inc |
| FEI number | 2023561 |
| Address | 130 Lombard St |
| City | Oxnard |
| State | CA |
| ZIP | 93030-5110 |
| Fiscal year | 2001 |
| Inspection end date | Nov 30, 2000 |
| Project area | Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| 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