FDA Inspection 857500 — Lisi Medical Orthopaedics

Lisi Medical Orthopaedics — FEI 3008556682

The FDA completed an inspection of Lisi Medical Orthopaedics on Nov 15, 2013 in Herouville-Saint-Clair. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Nov 15, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Herouville-Saint-Clair (France)

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