FDA Inspection 867793 — Hyphen BioMed Sasu

Hyphen BioMed Sasu — FEI 3004434070

The FDA completed an inspection of Hyphen BioMed Sasu on Feb 13, 2014 in Neuville-Sur-Oise. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Feb 13, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Neuville-Sur-Oise (France)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.