# FDA Inspection 1063470 - Lumanosity Inc - August 24, 2018

Source: https://www.keypedia.com/records/fda_inspections/lumanosity-inc/449cf9f3-2fbd-4fa3-b279-d78c1eba7a1f
Source feed: FDA_Inspections

> FDA Inspection 1063470 for Lumanosity Inc on August 24, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063470
- Company Name: Lumanosity Inc
- Inspection Date: 2018-08-24
- 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/lumanosity-inc/573b2c5e-4046-47e0-aa8b-c68f421b7c28

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