FDA inspection
Electro-tech Products, Inc.: FDA inspection ending Feb 17, 2009
FDA inspection 558505 · Official Action Indicated (OAI) · Glendora, CA
Key facts
| Inspection ID | 558505 |
|---|---|
| Firm | Electro-tech Products, Inc. |
| FEI number | 2023825 |
| Address | 2001 E Gladstone St Ste A |
| City | Glendora |
| State | CA |
| ZIP | 91740 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Feb 17, 2009 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| 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