FDA Inspection 844025 — Rayence Co. Ltd.

Rayence Co. Ltd. — FEI 3009048384

The FDA completed an inspection of Rayence Co. Ltd. on Jul 16, 2013 in Hwaseong. 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
Jul 16, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Hwaseong (Korea (the Republic of))

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