# FDA Inspection 1110661 - Solo-Dex LLC - November 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/solo-dex-llc/3d62330a-d547-4d74-a1fb-356bf0ecd895
Source feed: FDA_Inspections

> FDA Inspection 1110661 for Solo-Dex LLC on November 14, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1110661
- Company Name: Solo-Dex LLC
- Inspection Date: 2019-11-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/solo-dex-llc/32dcc2e4-65b2-4385-9c9c-0a4baaddf8f6

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