FDA Inspection 1080448 — Ventec Life Systems, Inc.
The FDA completed an inspection of Ventec Life Systems, Inc. on February 7, 2019 in Bothell, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 7, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bothell, WA (United States)