FDA Inspection 867793 — Hyphen BioMed sasu

Hyphen BioMed sasu — FEI 3004434070

The FDA completed an inspection of Hyphen BioMed sasu on February 13, 2014 in Neuville-Sur-Oise. 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
February 13, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Neuville-Sur-Oise (France)