FDA Inspection 1325874 — Ventec Life Systems, Inc.

Ventec Life Systems, Inc. — FEI 3017520736

The FDA completed an inspection of Ventec Life Systems, Inc. on July 8, 2026 in Woodinville, 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
July 8, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Woodinville, WA (United States)