# FDA Inspection 1095016 - Allwell Medical Corporation - July 02, 2019

Source: https://www.keypedia.com/records/fda_inspections/allwell-medical-corporation/ec92f735-da59-4ba2-bb53-e0a2d646b6b8
Source feed: FDA_Inspections

> FDA Inspection 1095016 for Allwell Medical Corporation on July 02, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095016
- Company Name: Allwell Medical Corporation
- Inspection Date: 2019-07-02
- 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/allwell-medical-corporation/8342dffd-678d-4882-a3ff-079d39e495e1

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