FDA Inspection 1288112 — MEMED US INC.

MEMED US INC. — FEI 3025785861

The FDA completed an inspection of MEMED US INC. on September 30, 2025 in Andover, MA. 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
September 30, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Andover, MA (United States)