FDA Inspection 1122361 — Cirtec Medical

Cirtec Medical — FEI 3004737415

The FDA completed an inspection of Cirtec Medical on January 27, 2020 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
January 27, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Clara, CA (United States)