FDA inspection
Neotech Products, LLC: FDA inspection ending Nov 10, 2014
FDA inspection 904331 · No Action Indicated (NAI) · Valencia, CA
Key facts
| Inspection ID | 904331 |
|---|---|
| Firm | Neotech Products, LLC |
| FEI number | 2025917 |
| Address | 28430 Witherspoon Pkwy |
| City | Valencia |
| State | CA |
| ZIP | 91355 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Nov 10, 2014 |
| 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