FDA Inspection 1175523 — ARCH Medical Solutions - Memphis

ARCH Medical Solutions - Memphis — FEI 3009973505

The FDA completed an inspection of ARCH Medical Solutions - Memphis on July 8, 2022 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
July 8, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Bartlett, TN (United States)