FDA Inspection 894203 — Gexfix SA

Gexfix SA — FEI 3005157180

The FDA completed an inspection of Gexfix SA on September 4, 2014 in Le Grand-Saconnex. 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
September 4, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Le Grand-Saconnex (Switzerland)