FDA Inspection 1233654 — MIRIS AB

MIRIS AB — FEI 3013887826

The FDA completed an inspection of MIRIS AB on Feb 15, 2024 in Uppsala. 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
Feb 15, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Uppsala (Sweden)