FDA inspection
Remel, Inc: FDA inspection ending Mar 3, 2023
FDA inspection 1199839 · No Action Indicated (NAI) · Lenexa, KS
Key facts
| Inspection ID | 1199839 |
|---|---|
| Firm | Remel, Inc |
| FEI number | 1924669 |
| Address | 12076 Santa Fe Trail Dr |
| City | Lenexa |
| State | KS |
| ZIP | 66215 |
| Country | United States |
| Fiscal year | 2023 |
| Inspection end date | Mar 3, 2023 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 10–99 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