# Lumasense Technologies, Inc. – FDA Inspection, Aug 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 of Lumasense Technologies, Inc., August 28, 2013. Classification: Voluntary Action Indicated (VAI). 11 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 11

## Related Documents

- [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