FDA Inspection 1124379 — Curatia Medical Co

Curatia Medical Co — FEI 3008361782

The FDA completed an inspection of Curatia Medical Co on February 3, 2020 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
February 3, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunnyvale, CA (United States)