FDA Inspection 1277035 — Biocartis Nv

Biocartis Nv — FEI 3009972873

The FDA completed an inspection of Biocartis Nv on Jul 3, 2025 in Mechelen. 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 3, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mechelen (Belgium)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.