FDA Inspection 1199429 — Cirtec Medical

Cirtec Medical — FEI 3004737415

The FDA completed an inspection of Cirtec Medical on March 8, 2023 in Santa Clara, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 8, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Clara, CA (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures