FDA Inspection 986695 — Eb Neuro Spa

Eb Neuro Spa — FEI 3001687738

The FDA completed an inspection of Eb Neuro Spa on May 6, 2016 in Negrar. 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 6, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Negrar (Italy)

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