# FDA Inspection 906360 - Wellell Inc - November 07, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/wellell-inc/fd38c509-34b0-4a49-8839-bb5a4054c24f/
Source feed: FDA_Inspections

> FDA Inspection 906360 for Wellell Inc on November 07, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 906360
- Company Name: Wellell Inc
- Inspection Date: 2014-11-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 773367 - 2012-02-23](https://www.globalkeysolutions.net/api/records/fda_inspections/wellell-inc/3eb45a38-fbd5-445c-b42f-d138f35c93a4/)
- [FDA Inspection 773367 - 2012-02-23](https://www.globalkeysolutions.net/api/records/fda_inspections/wellell-inc/a8acef32-8bf7-46a8-92f3-a156bae96385/)

Company: https://www.globalkeysolutions.net/companies/wellell-inc/464e2887-72c4-473d-bb30-b384b75febaf

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