FDA Import Refusal AEK-9633465-9/80002/1 — LUMINOVA PHARMA GROUP

LUMINOVA PHARMA GROUP — FEI 3044830120

The FDA refused shipment AEK-9633465-9/80002/1 from LUMINOVA PHARMA GROUP (Guatemala) on Sep 3, 2026. The refused product falls under Drugs and Biologics — AMOXICILLIN TRIHYDRATE (PENICILLIN, SYNTHETICALLY PRODUCED). Cited charge: 75 This firm has 2 other import refusals on record.

Refusal Details

Date
Sep 3, 2026
Country
Guatemala
Product Category
Drugs and Biologics
Product Code
56BDA03 AMOXICILLIN TRIHYDRATE (PENICILLIN, SYNTHETICALLY PRODUCED)
Charges
75