FDA Inspection 1319382 — ABMRC, LLC

ABMRC, LLC — FEI 3016774528

The FDA completed an inspection of ABMRC, LLC on May 21, 2026 in Eagan, MN. 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 21, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Eagan, MN (United States)