FDA Import Refusal FR1-0018063-2/11/1 — LETSMED GMBH

LETSMED GMBH — FEI 3015283038

The FDA refused shipment FR1-0018063-2/11/1 from LETSMED GMBH (Germany) on Dec 28, 2020. The refused product falls under Devices — SET, ADMINISTRATION, INTRAVASCULAR. Cited charge: 118 This firm has 2 other import refusals on record.

Refusal Details

Date
Dec 28, 2020
Country
Germany
Product Category
Devices
Product Code
80FPA SET, ADMINISTRATION, INTRAVASCULAR
Charges
118

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