FDA Inspection
Relevium Labs IncRelevium Labs Inc – FDA Inspection, Oct 20, 2017
Record Details
This FDA Inspection record concerns Relevium Labs Inc, with an inspection on October 20, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Teresa K. Kastner
View Company Profile
ID · c713c4de-a77a-4cde-ad7c-6fe55afd5ce3
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1031109
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Relevium Labs Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 12, 2025 | NAI | Postmarket Assurance: Devices | |
| August 31, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Relevium Labs Inc
- FDA Inspection 1261641 - 2025-02-12
- FDA Inspection 1179394 - 2022-08-31
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.