# FDA Inspection 847589 - Lumasense Technologies, Inc. - August 28, 2013

Source: https://www.keypedia.com/records/fda_inspections/lumasense-technologies-inc/58eec2c7-fe3d-40c2-9fb5-29d5080c3211
Source feed: FDA_Inspections

> FDA Inspection 847589 for Lumasense Technologies, Inc. on August 28, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 847589
- Company Name: Lumasense Technologies, Inc.
- Inspection Date: 2013-08-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 847589 - 2013-08-28](https://www.keypedia.com/records/fda_inspections/lumasense-technologies-inc/1e2bc34a-f39a-457b-a29f-058298431fca)
- [FDA Inspection 660358 - 2010-04-16](https://www.keypedia.com/records/fda_inspections/lumasense-technologies-inc/a984fc62-b74f-4195-85c4-86b39a51935f)
- [FDA Inspection 660358 - 2010-04-16](https://www.keypedia.com/records/fda_inspections/lumasense-technologies-inc/f4c0fc06-69fa-4152-946a-d75c3c070e4e)

Company: https://www.keypedia.com/companies/lumasense-technologies-inc/f18c3e5b-f9f1-4eaa-943e-b4720f3ab105

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