FDA Inspection 911564 — Vipamat SAS

Vipamat SAS — FEI 3005442882

The FDA completed an inspection of Vipamat SAS on Dec 4, 2014 in Ploemeur. 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
Dec 4, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Ploemeur (France)

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