FDA Inspection 1165219 — Venclose, Inc.

Venclose, Inc. — FEI 3011879048

The FDA completed an inspection of Venclose, Inc. on Feb 25, 2022 in San Jose, CA. 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
Feb 25, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Jose, CA (United States)