FDA inspection
Multiline Technology Inc.: FDA inspection ending Nov 15, 1999
FDA inspection 3595 · No Action Indicated (NAI) · Farmingdale, NY
Key facts
| Inspection ID | 3595 |
|---|---|
| Firm | Multiline Technology Inc. |
| FEI number | 1000119668 |
| Address | 400 Broadhollow Rd |
| City | Farmingdale |
| State | NY |
| ZIP | 11735-4824 |
| Fiscal year | 2000 |
| Inspection end date | Nov 15, 1999 |
| Classification | No Action Indicated (NAI) |
| 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