FDA Inspection 1246801 — PIXEE MEDICAL

PIXEE MEDICAL — FEI 3020703212

The FDA completed an inspection of PIXEE MEDICAL on Jul 25, 2024 in Besancon. 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 25, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Besancon (France)