FDA inspection
KESTRA MEDICAL TECHNOLOGIES, INC.: FDA inspection ending Oct 15, 2020
FDA inspection 1132681 · No Action Indicated (NAI) · Kirkland, WA
Key facts
| Inspection ID | 1132681 |
|---|---|
| Firm | KESTRA MEDICAL TECHNOLOGIES, INC. |
| FEI number | 3015185344 |
| Address | 3933 Lake Washington Blvd Ne |
| City | Kirkland |
| State | WA |
| ZIP | 98033 |
| Country | United States |
| Fiscal year | 2021 |
| Inspection end date | Oct 15, 2020 |
| 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