# FDA Inspection 1113121 - Liberty Engineering Inc - December 18, 2019

Source: https://www.keypedia.com/records/fda_inspections/liberty-engineering-inc/3d54629b-8e89-4855-b4e0-1b05a9fbc1cc
Source feed: FDA_Inspections

> FDA Inspection 1113121 for Liberty Engineering Inc on December 18, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1113121
- Company Name: Liberty Engineering Inc
- Inspection Date: 2019-12-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1113121 - 2019-12-18](https://www.keypedia.com/records/fda_inspections/liberty-engineering-inc/06fb0582-1ad5-4954-9730-aafecc8bc2dd)
- [FDA Inspection 859382 - 2013-12-18](https://www.keypedia.com/records/fda_inspections/liberty-engineering-inc/c18ee254-df48-4f66-a000-969fb39335eb)
- [FDA Inspection 648648 - 2010-02-23](https://www.keypedia.com/records/fda_inspections/liberty-engineering-inc/08c9547a-0662-4480-bb1c-d9a921ed7e4a)

Company: https://www.keypedia.com/companies/liberty-engineering-inc/1071260f-f98f-4e6c-bcbc-e863e30d79bf

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