FDA inspection
Laseraim Tools, Inc: FDA inspection ending Apr 12, 2000
FDA inspection 20361 · Voluntary Action Indicated (VAI) · Little Rock, AR
Key facts
| Inspection ID | 20361 |
|---|---|
| Firm | Laseraim Tools, Inc |
| FEI number | 3002987806 |
| Address | 6600 Geyer Springs Rd |
| City | Little Rock |
| State | AR |
| ZIP | 72209-2722 |
| Fiscal year | 2000 |
| Inspection end date | Apr 12, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| 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