FDA inspection
Cymer, Inc: FDA inspection ending Aug 29, 2005
FDA inspection 393591 · San Diego, CA
Key facts
| Inspection ID | 393591 |
|---|---|
| Firm | Cymer, Inc |
| FEI number | 2027229 |
| Address | 17075 Thornmint Ct |
| City | San Diego |
| State | CA |
| ZIP | 92127-2413 |
| Fiscal year | 2005 |
| Inspection end date | Aug 29, 2005 |
| Project area | Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| 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