FDA Inspection 1201923 — CXMedUS, Inc.

CXMedUS, Inc. — FEI 3023058994

The FDA completed an inspection of CXMedUS, Inc. on April 6, 2023 in Grand Blanc, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 6, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Grand Blanc, MI (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
63021 CFR 803.17Lack of Written MDR Procedures