# FDA Inspection 1169181 - Reliance Mobility, LLC - May 09, 2022

Source: https://www.keypedia.com/records/fda_inspections/reliance-mobility-llc/cce3df99-cfd0-4269-8aa1-45a6871cbd66
Source feed: FDA_Inspections

> FDA Inspection 1169181 for Reliance Mobility, LLC on May 09, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1169181
- Company Name: Reliance Mobility, LLC
- Inspection Date: 2022-05-09
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1169181 - 2022-05-09](https://www.keypedia.com/records/fda_inspections/reliance-mobility-llc/bb784487-0ad8-46a6-ae1d-c940ee7d1b76)
- [FDA Inspection 1047864 - 2018-04-10](https://www.keypedia.com/records/fda_inspections/reliance-mobility-llc/abfe32f7-e3cc-49d8-a544-ca36f05f9641)
- [FDA Inspection 1047864 - 2018-04-10](https://www.keypedia.com/records/fda_inspections/reliance-mobility-llc/10be924f-786f-4f0e-9542-39ae15975c16)

Company: https://www.keypedia.com/companies/reliance-mobility-llc/9cd42cd4-ea6b-4de3-8368-ba6893072778

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