# FDA Inspection 954813 - Lutronic Corporation - October 29, 2015

Source: https://www.keypedia.com/records/fda_inspections/lutronic-corporation/8e7c870e-456a-4cef-8643-3f64b40811a9
Source feed: FDA_Inspections

> FDA Inspection 954813 for Lutronic Corporation on October 29, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 954813
- Company Name: Lutronic Corporation
- Inspection Date: 2015-10-29
- 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 954813 - 2015-10-29](https://www.keypedia.com/records/fda_inspections/lutronic-corporation/541cf611-814c-4505-a535-c2b4d1be6229)
- [FDA Inspection 954813 - 2015-10-29](https://www.keypedia.com/records/fda_inspections/lutronic-corporation/4dde11fd-d7c4-4475-84b4-82a905ee73a0)

Company: https://www.keypedia.com/companies/lutronic-corporation/f9c8b6b8-78fa-4707-8d73-5401533402b2

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