FDA Inspection 1248326 — SUBAN Instruments Hungary Co

SUBAN Instruments Hungary Co — FEI 3002631673

The FDA completed an inspection of SUBAN Instruments Hungary Co on Jul 10, 2024 in Debrecen. 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
Jul 10, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Debrecen (Hungary)