# FDA Inspection 1085715 - Livermoretech, Inc. - March 20, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/livermoretech-inc/27b34e1c-4ffb-465b-a573-1f2fd476a6b6
Source feed: FDA_Inspections

> FDA Inspection 1085715 for Livermoretech, Inc. on March 20, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1085715
- Company Name: Livermoretech, Inc.
- Inspection Date: 2019-03-20
- 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 1085715 - 2019-03-20](https://www.globalkeysolutions.net/records/fda_inspections/livermoretech-inc/4368095a-d991-4486-af11-a040eae980b0)
- [FDA Inspection 1085715 - 2019-03-20](https://www.globalkeysolutions.net/records/fda_inspections/livermoretech-inc/88414d1e-8cb5-4538-9677-d959219262c3)

Company: https://www.globalkeysolutions.net/companies/livermoretech-inc/cfe680f5-445c-48e0-8152-c3a966f21350

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