FDA Inspection 1132681 — KESTRA MEDICAL TECHNOLOGIES, INC.
The FDA completed an inspection of KESTRA MEDICAL TECHNOLOGIES, INC. on Oct 15, 2020 in Kirkland, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Oct 15, 2020
- Fiscal Year
- 2021
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kirkland, WA (United States)