FDA Inspection 988479 — Sentinel CH SpA

Sentinel CH SpA — FEI 3000303338

The FDA completed an inspection of Sentinel CH SpA on Sep 22, 2016 in Milan. 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
Sep 22, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Milan (Italy)

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