# Livermoretech, Inc. – FDA Inspection, Mar 20, 2019

Source: https://www.keypedia.com/records/fda_inspections/livermoretech-inc/88414d1e-8cb5-4538-9677-d959219262c3
Source feed: FDA_Inspections

> FDA inspection 1085715 of Livermoretech, Inc., 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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

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

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