# FDA Inspection 950736 - Advalight ApS - November 26, 2015

Source: https://www.keypedia.com/records/fda_inspections/advalight-aps/12aa6c5e-617e-4740-944c-878acab804c4
Source feed: FDA_Inspections

> FDA Inspection 950736 for Advalight ApS on November 26, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 950736
- Company Name: Advalight ApS
- Inspection Date: 2015-11-26
- 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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Company: https://www.keypedia.com/companies/advalight-aps/a67b50d1-6457-422c-ae66-d15e2aa1369b

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