FDA Import Refusal EAA-0017794-1/11/1 — Acomma Co., Ltd.

Acomma Co., Ltd. — FEI 3013682164

The FDA refused shipment EAA-0017794-1/11/1 from Acomma Co., Ltd. (South Korea) on Sep 6, 2017. The refused product falls under Devices — PADS, MENSTRUAL, SCENTED-DEODORIZED. Cited charges: 3280,341

Refusal details

Date
Sep 6, 2017
Country
South Korea
Product Category
Devices
Product Code
85NRC PADS, MENSTRUAL, SCENTED-DEODORIZED
Charges
3280,341

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