FDA Import Refusal 799-5669057-6/1/1 — MIKUNI KOGYO CO LTD. KOHAN PLANT

MIKUNI KOGYO CO LTD. KOHAN PLANT — FEI 3008069922

The FDA refused shipment 799-5669057-6/1/1 from MIKUNI KOGYO CO LTD. KOHAN PLANT (Japan) on Aug 28, 2014. The refused product falls under Devices — NEEDLE, DENTAL. Cited charge: 118

Refusal details

Date
Aug 28, 2014
Country
Japan
Product Category
Devices
Product Code
76DZM NEEDLE, DENTAL
Charges
118

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