FDA Inspection 1175373 — Curemetrix, Inc.

Curemetrix, Inc. — FEI 3017173128

The FDA completed an inspection of Curemetrix, Inc. on Jun 15, 2022 in San Diego, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 15, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)