FDA Inspection 820118 — Gexfix SA

Gexfix SA — FEI 3005157180

The FDA completed an inspection of Gexfix SA on January 16, 2013 in Le Grand-Saconnex. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
January 16, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Le Grand-Saconnex (Switzerland)