FDA Inspection 1085715 — Livermoretech, Inc.
The FDA completed an inspection of Livermoretech, Inc. on March 20, 2019 in Plano, TX. 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
- March 20, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Plano, TX (United States)