FDA Import Refusal 799-4627179-8/11/1 — Indivumed Gmbh

Indivumed Gmbh — FEI 3008388552

The FDA refused shipment 799-4627179-8/11/1 from Indivumed Gmbh (Germany) on May 26, 2023. The refused product falls under Devices — SCALPEL, ONE-PIECE. Cited charges: 118,3280,341

Refusal details

Date
May 26, 2023
Country
Germany
Product Category
Devices
Product Code
79GDX SCALPEL, ONE-PIECE
Charges
118,3280,341

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