# Allwell Medical Corporation – FDA Inspection, Jul 2, 2019

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

> FDA inspection 1095016 of Allwell Medical Corporation, July 02, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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- FDA Inspection 890938 - 2014-07-23
- [FDA Inspection 736566 - 2011-07-20](https://www.keypedia.com/records/fda_inspections/allwell-medical-corporation/c6e6f4ba-b048-48f9-8d12-09fb0def88aa)

## Related Officers

- [Investigator](https://www.keypedia.com/people/dawn-m-braswell/6a66fdbb-fff8-4b4b-9f06-320464957b87)

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