FDA Inspection 1316016 — Cirtec Medical

Cirtec Medical — FEI 3004737415

The FDA completed an inspection of Cirtec Medical on April 23, 2026 in Santa Clara, CA. 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
April 23, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Clara, CA (United States)