FDA Inspection 1277413 — Corvent Medical, Inc.

Corvent Medical, Inc. — FEI 3033571078

The FDA completed an inspection of Corvent Medical, Inc. on June 25, 2025 in Fargo, ND. 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
June 25, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Fargo, ND (United States)