FDA Inspection 1034634 — Diadent Group International

Diadent Group International — FEI 3010138769

The FDA completed an inspection of Diadent Group International on Nov 23, 2017 in Cheongju. 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 23, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Cheongju (Korea (the Republic of))

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