# FDA Inspection 593981 - LXE,  Inc. - June 24, 2009

Source: https://www.keypedia.com/records/fda_inspections/lxe-inc/c237275e-9ecf-426e-8f1f-bea784b6aa46
Source feed: FDA_Inspections

> FDA Inspection 593981 for LXE,  Inc. on June 24, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 593981
- Company Name: LXE,  Inc.
- Inspection Date: 2009-06-24
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/lxe-inc/deaedf3c-c868-4a33-91c7-f79c3a24463b

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