FDA Inspection 1180656 — Relievant Medsystems, Inc.

Relievant Medsystems, Inc. — FEI 3006789852

The FDA completed an inspection of Relievant Medsystems, Inc. on Jun 23, 2022 in Sunnyvale, 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 23, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunnyvale, CA (United States)