FDA Inspection 1191982 — MatOrtho Ltd

MatOrtho Ltd — FEI 3008985661

The FDA completed an inspection of MatOrtho Ltd on Nov 3, 2022 in Leatherhead. 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 3, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Leatherhead (United Kingdom)

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