FDA inspection
TIDI Products, LLC: FDA inspection ending Nov 27, 2012
FDA inspection 809068 · No Action Indicated (NAI) · Neenah, WI
Key facts
| Inspection ID | 809068 |
|---|---|
| Firm | TIDI Products, LLC |
| FEI number | 2182318 |
| Address | 570 Enterprise Dr |
| City | Neenah |
| State | WI |
| ZIP | 54956 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Nov 27, 2012 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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