FDA Import Refusal 799-4025845-0/11/1 — NINGBO KML

NINGBO KML — FEI 3015220085

The FDA refused shipment 799-4025845-0/11/1 from NINGBO KML (China) on Nov 7, 2019. The refused product falls under Devices — HUMIDIFIER, RESPIRATORY, MASK (DIRECT PATIENT INTERFACE). Cited charges: 118,3280,341 This firm has 1 other import refusal on record.

Refusal details

Date
Nov 7, 2019
Country
China
Product Category
Devices
Product Code
73OBN HUMIDIFIER, RESPIRATORY, MASK (DIRECT PATIENT INTERFACE)
Charges
118,3280,341

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