FDA inspection
KREWE DU OPTIC: FDA inspection ending Nov 1, 2016
FDA inspection 1017591 · No Action Indicated (NAI) · New Orleans, LA
Key facts
| Inspection ID | 1017591 |
|---|---|
| Firm | KREWE DU OPTIC |
| FEI number | 3012119296 |
| Address | 1020 Thalia St |
| City | New Orleans |
| State | LA |
| ZIP | 70130 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Nov 1, 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