FDA Import Refusal 799-4429901-6/12/1 — KUSDOM DESIGN GROUP LIMITED

KUSDOM DESIGN GROUP LIMITED — FEI 3032904543

The FDA refused shipment 799-4429901-6/12/1 from KUSDOM DESIGN GROUP LIMITED (Hong Kong) on Dec 19, 2024. The refused product falls under Devices — CHAMBER, OXYGEN, TOPICAL, EXTREMITY. Cited charge: 118 This firm has 2 other import refusals on record.

Refusal Details

Date
Dec 19, 2024
Country
Hong Kong
Product Category
Devices
Product Code
79KPJ CHAMBER, OXYGEN, TOPICAL, EXTREMITY
Charges
118

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