# FDA Inspection 1078716 - Televere Systems, LLC - November 29, 2018

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

> FDA Inspection 1078716 for Televere Systems, LLC on November 29, 2018. Classification: No Action Indicated (NAI).

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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)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1078716 - 2018-11-29](https://www.globalkeysolutions.net/records/fda_inspections/televere-systems-llc/70cfc5a5-095a-4f9a-8a4a-d430ec1b1d0b)
- [FDA Inspection 1078716 - 2018-11-29](https://www.globalkeysolutions.net/records/fda_inspections/televere-systems-llc/476ab772-1c3f-4647-98f2-da5a4fc3f466)

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

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