FDA Inspection 1040049 — Relievant Medsystems, Inc.
The FDA completed an inspection of Relievant Medsystems, Inc. on Jan 26, 2018 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
- Jan 26, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sunnyvale, CA (United States)