# FDA Inspection 1023339 - Lumen Photon Therapy Inc. - July 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/lumen-photon-therapy-inc/b706ff17-31d0-496f-8157-91e3bc4e6e44
Source feed: FDA_Inspections

> FDA Inspection 1023339 for Lumen Photon Therapy Inc. on July 13, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023339
- Company Name: Lumen Photon Therapy Inc.
- Inspection Date: 2017-07-13
- 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 1023339 - 2017-07-13](https://www.keypedia.com/records/fda_inspections/lumen-photon-therapy-inc/bb39832a-db1e-4778-bc7d-40d9b1f4ec88)
- [FDA Inspection 780575 - 2012-04-17](https://www.keypedia.com/records/fda_inspections/lumen-photon-therapy-inc/4249eeb2-37de-40bd-8066-5e2af5e5dd38)
- [FDA Inspection 780575 - 2012-04-17](https://www.keypedia.com/records/fda_inspections/lumen-photon-therapy-inc/87b31a03-24df-49db-9226-a20860d36e4a)

Company: https://www.keypedia.com/companies/lumen-photon-therapy-inc/b01da353-2639-48f3-9f69-cbf6afad2de8

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