FDA Inspection 749559 — Selenium Medical S.A.S.

Selenium Medical S.A.S. — FEI 1000461041

The FDA completed an inspection of Selenium Medical S.A.S. on Sep 21, 2011 in La Rochelle. 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 21, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
La Rochelle (France)