FDA Inspection 1224533 — Curatia Medical Co

Curatia Medical Co — FEI 3008361782

The FDA completed an inspection of Curatia Medical Co on December 4, 2023 in Sunnyvale, 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
December 4, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunnyvale, CA (United States)