FDA Inspection 1085862 — InTheSmart Co., Ltd.

InTheSmart Co., Ltd. — FEI 3014409527

The FDA completed an inspection of InTheSmart Co., Ltd. on Feb 12, 2019 in Jongro. 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
Feb 12, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Jongro (Korea (the Republic of))

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