FDA Inspection 1318312 — ARCH Medical Solutions - Memphis

ARCH Medical Solutions - Memphis — FEI 3009973505

The FDA completed an inspection of ARCH Medical Solutions - Memphis on May 7, 2026 in Bartlett, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 7, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Bartlett, TN (United States)