# FDA Inspection 1106042 - Wello, Inc. - October 10, 2019

Source: https://www.keypedia.com/records/fda_inspections/wello-inc/7c358441-634a-4533-ba55-e599ac5dd6a2
Source feed: FDA_Inspections

> FDA Inspection 1106042 for Wello, Inc. on October 10, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1106042
- Company Name: Wello, Inc.
- Inspection Date: 2019-10-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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