FDA Inspection 1206895 — CARTIHEAL, LTD

CARTIHEAL, LTD — FEI 3013881076

The FDA completed an inspection of CARTIHEAL, LTD on May 3, 2023 in Kfar Saba. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 3, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Kfar Saba (Israel)

Additional Details

Postmarket Audit Inspections