FDA Inspection 1251244 — Liko AB

Liko AB — FEI 3000230206

The FDA completed an inspection of Liko AB on Sep 5, 2024 in Lulea. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 5, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lulea (Sweden)