FDA Inspection 1191280 — Retia Medical Systems Inc

Retia Medical Systems Inc — FEI 3015418961

The FDA completed an inspection of Retia Medical Systems Inc on October 14, 2022 in Valhalla, NY. 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
October 14, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Valhalla, NY (United States)