FDA inspection
Eagle Electrode Manufacturing LLC: FDA inspection ending Dec 15, 2016
FDA inspection 995760 · No Action Indicated (NAI) · Ijamsville, MD
Key facts
| Inspection ID | 995760 |
|---|---|
| Firm | Eagle Electrode Manufacturing LLC |
| FEI number | 3009492424 |
| Address | 10075 Tyler Ct Ste 11 |
| City | Ijamsville |
| State | MD |
| ZIP | 21754 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Dec 15, 2016 |
| 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