FDA Inspection 1031109 — Relevium Labs Inc
The FDA completed an inspection of Relevium Labs Inc on Oct 20, 2017 in Oxford, OH. 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
- Oct 20, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Oxford, OH (United States)