# Mid-America Medical Innovations, LLC. – FDA Inspection, Dec 5, 2017

Source: https://www.keypedia.com/records/fda_inspections/mid-america-medical-innovations-llc/7b4a4e7b-17f6-4555-8d88-86711cf40e20
Source feed: FDA_Inspections

> FDA inspection 1033895 of Mid-America Medical Innovations, LLC., December 05, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1033895
- Company Name: Mid-America Medical Innovations, LLC.
- Inspection Date: 2017-12-05
- 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: 2

## Related Officers

- [Investigator](https://www.keypedia.com/people/eric-c-fox/218af117-1551-476f-80ba-172e2cd6baee)

Company: https://www.keypedia.com/companies/mid-america-medical-innovations-llc/e7ea0d31-580f-42ef-b6c2-32e7009120fc

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