FDA Inspection 1274117 — ELITechGroup MDX LLC.

ELITechGroup MDX LLC. — FEI 3003540236

The FDA completed an inspection of ELITechGroup MDX LLC. on June 27, 2025 in Bothell, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 27, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bothell, WA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures