Home / Import refusals / FR1-0019175-3/13/1

FDA Import Refusal FR1-0019175-3/13/1 — LETSMED GMBH

LETSMED GMBH — FEI 3036370027

The FDA refused shipment FR1-0019175-3/13/1 from LETSMED GMBH (Germany) on Apr 9, 2025. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charges: 118,3280 This firm has 2 other import refusals on record.

Refusal Details

Date
Apr 9, 2025
Country
Germany
Product Category
Devices
Product Code
80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
Charges
118,3280

Other import refusals

FDA data resources

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