FDA inspection
TIDI Products, LLC: FDA inspection ending Nov 7, 2005
FDA inspection 410927 · No Action Indicated (NAI) · Neenah, WI
Key facts
| Inspection ID | 410927 |
|---|---|
| Firm | TIDI Products, LLC |
| FEI number | 2182318 |
| Address | 570 Enterprise Dr |
| City | Neenah |
| State | WI |
| ZIP | 54956-4865 |
| Fiscal year | 2006 |
| Inspection end date | Nov 7, 2005 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| 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