FDA inspection
Enova Illumination Inc: FDA inspection ending May 29, 2002
FDA inspection 223480 · No Action Indicated (NAI) · Minneapolis, MN
Key facts
| Inspection ID | 223480 |
|---|---|
| Firm | Enova Illumination Inc |
| FEI number | 2127132 |
| Address | 1717 Broadway St Ne |
| City | Minneapolis |
| State | MN |
| ZIP | 55413-2638 |
| Fiscal year | 2002 |
| Inspection end date | May 29, 2002 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med 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