FDA inspection
Micro Laser Systems: FDA inspection ending Mar 28, 2007
FDA inspection 467653 · Garden Grove, CA
Key facts
| Inspection ID | 467653 |
|---|---|
| Firm | Micro Laser Systems |
| FEI number | 2027137 |
| Address | 12841 Western Ave Ste H |
| City | Garden Grove |
| State | CA |
| ZIP | 92841-4025 |
| Fiscal year | 2007 |
| Inspection end date | Mar 28, 2007 |
| 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