# FDA Inspection 813140 - Xlumena, Inc. - January 16, 2013

Source: https://www.keypedia.com/records/fda_inspections/xlumena-inc/2e8cab7d-2e4b-486d-b2ac-0dda895335fd
Source feed: FDA_Inspections

> FDA Inspection 813140 for Xlumena, Inc. on January 16, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 813140
- Company Name: Xlumena, Inc.
- Inspection Date: 2013-01-16
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 940242 - 2015-08-28](https://www.keypedia.com/records/fda_inspections/xlumena-inc/c0af99db-31d5-42a5-afac-5ed9e45bd6b8)
- [FDA Inspection 813140 - 2013-01-16](https://www.keypedia.com/records/fda_inspections/xlumena-inc/f0a33e84-5ccb-41e3-a2fe-8ae240a567c5)

Company: https://www.keypedia.com/companies/xlumena-inc/30ba162f-e4fc-4e8d-9505-45fd2671e69e

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