FDA Inspection 1328418 — IQ Products BV

IQ Products BV — FEI 3002807541

The FDA completed an inspection of IQ Products BV on May 14, 2026 in Groningen. 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
May 14, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Groningen (Netherlands)

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