FDA Inspection 823449 — Graftys

Graftys — FEI 3006761298

The FDA completed an inspection of Graftys on Mar 7, 2013 in LYON. 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
Mar 7, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
LYON (France)

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