FDA Inspection 1206769 — DreamCon Co. Ltd.

DreamCon Co. Ltd. — FEI 3010460316

The FDA completed an inspection of DreamCon Co. Ltd. on May 11, 2023 in Yangsan. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 11, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Yangsan (Korea (the Republic of))

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