FDA Inspection 1277413 — Corvent Medical, Inc.

Corvent Medical, Inc. — FEI 3033571078

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.