# Televere Systems, LLC – FDA Inspection, Nov 29, 2018

Source: https://www.keypedia.com/records/fda_inspections/televere-systems-llc/d3e60262-9276-4ea4-b4d8-6a531d3a28ea
Source feed: FDA_Inspections

> FDA inspection 1078716 of Televere Systems, LLC, November 29, 2018. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1078716
- Company Name: Televere Systems, LLC
- Inspection Date: 2018-11-29
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1314798 - 2026-04-22](https://www.keypedia.com/records/fda_inspections/televere-systems-llc/e87c970e-5e3e-4689-a2b5-ea7c5f73a2f3)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/jennifer-s-ness/532f8a81-e393-4e83-b5f2-a72362e966de)

Company: https://www.keypedia.com/companies/televere-systems-llc/e585c21e-2bab-4be8-ab6f-8c7e57314594

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7