FDA Inspection 1190646 — Elekta Inc

Elekta Inc — FEI 1937649

The FDA completed an inspection of Elekta Inc on Sep 16, 2022 in Saint Charles, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 16, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Charles, MO (United States)