FDA Inspection 1033895 — Mid-America Medical Innovations, LLC.

Mid-America Medical Innovations, LLC. — FEI 3011624421

The FDA completed an inspection of Mid-America Medical Innovations, LLC. on Dec 5, 2017 in Jefferson City, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 5, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jefferson City, MO (United States)

Citations

IDCFRDescription
312721 CFR 820.80(e)Documentation
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures