FDA Inspection
Televere Systems, LLCTelevere Systems, LLC – FDA Inspection, Apr 22, 2026
Record Details
This FDA Inspection record concerns Televere Systems, LLC, with an inspection on April 22, 2026, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · e87c970e-5e3e-4689-a2b5-ea7c5f73a2f3
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1314798
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
- 21 CFR 820.181DMR - not or inadequately maintained
- ISO 13485:2016 Clause 7.1Product realization risk management processes not documented
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Televere Systems, LLC
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 29, 2018 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Televere Systems, LLC
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.