FDA inspection
Resonance Technology Inc: FDA inspection ending Jul 17, 2019
FDA inspection 1099478 · No Action Indicated (NAI) · Northridge, CA
Key facts
| Inspection ID | 1099478 |
|---|---|
| Firm | Resonance Technology Inc |
| FEI number | 1000306474 |
| Address | 18121 Parthenia St |
| City | Northridge |
| State | CA |
| ZIP | 91325 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Jul 17, 2019 |
| 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