FDA Import Refusal AEK-9488425-9/10002/1 — SmartPractice Europe GmbH
The FDA refused shipment AEK-9488425-9/10002/1 from SmartPractice Europe GmbH (Germany) on Feb 27, 2026. The refused product falls under Drugs and Biologics — IN-VITRO DIAG PRODUCTS, N.E.C.. Cited charges: 118,2280,71,75
Refusal details
- Date
- Feb 27, 2026
- Country
- Germany
- Product Category
- Drugs and Biologics
- Product Code
- 57VY99 IN-VITRO DIAG PRODUCTS, N.E.C.
- Charges
- 118,2280,71,75