FDA Inspection 1292256 — Implantica CE Reflux Ltd

Implantica CE Reflux Ltd — FEI 3015217460

The FDA completed an inspection of Implantica CE Reflux Ltd on Oct 24, 2025 in San Gwann. 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
Oct 24, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
San Gwann (Malta)

Additional Details

Sponsor, Contract Research Organization

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