FDA Import Refusal 224-4306750-3/43/3 — K.K. Hakugen

K.K. Hakugen — FEI 3000291935

The FDA refused shipment 224-4306750-3/43/3 from K.K. Hakugen (Japan) on Oct 4, 2007. The refused product falls under Devices — DEVICE, GENERAL MEDICAL. Cited charges: 3260,341 This firm has 2 other import refusals on record.

Refusal details

Date
Oct 4, 2007
Country
Japan
Product Category
Devices
Product Code
80LDQ DEVICE, GENERAL MEDICAL
Charges
3260,341

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