FDA Inspection
Trividia Health, Inc.Trividia Health, Inc. – FDA Inspection, Jun 22, 2017
Record Details
This FDA Inspection record concerns Trividia Health, Inc., with an inspection on June 22, 2017, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · d51fa77b-2cdb-4d67-98d3-cf5058864717
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1015197
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 803.17(a)(1)Lack of System for Event Evaluations
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Trividia Health, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| July 21, 2025 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
| June 27, 2014 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 15, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Trividia Health, Inc.
- FDA Inspection 1277857 - 2025-07-21
- FDA Inspection 886183 - 2014-06-27
- FDA Inspection 819603 - 2013-02-15
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.