FDA Inspection 1078716 — Televere Systems, LLC
The FDA completed an inspection of Televere Systems, LLC on November 29, 2018 in Janesville, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 29, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Janesville, WI (United States)