# FDA Inspection 1208493 - Wello, Inc. - June 21, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/wello-inc/fd5bfea1-96f0-4e8c-9cc5-56dc18221051/
Source feed: FDA_Inspections

> FDA Inspection 1208493 for Wello, Inc. on June 21, 2023. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1208493
- Company Name: Wello, Inc.
- Inspection Date: 2023-06-21
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1208493 - 2023-06-21](https://www.globalkeysolutions.net/api/records/fda_inspections/wello-inc/ef713a68-7ba2-454e-80ff-260da7b52b7d/)
- [FDA Inspection 1106042 - 2019-10-10](https://www.globalkeysolutions.net/api/records/fda_inspections/wello-inc/7c358441-634a-4533-ba55-e599ac5dd6a2/)
- [FDA Inspection 1106042 - 2019-10-10](https://www.globalkeysolutions.net/api/records/fda_inspections/wello-inc/a0b0c10f-d75b-4410-936f-3ae7d85954ec/)

Company: https://www.globalkeysolutions.net/companies/wello-inc/68dcd1f8-7caa-4e95-9a5c-18304b888271

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