FDA Inspection 911564 — Vipamat SAS

Vipamat SAS — FEI 3005442882

The FDA completed an inspection of Vipamat SAS on December 4, 2014 in Ploemeur. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 4, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Ploemeur (France)