FDA Import Refusal AEK-2302643-7/30003/1 — LUMINOVA PHARMA GROUP

LUMINOVA PHARMA GROUP — FEI 3044830120

The FDA refused shipment AEK-2302643-7/30003/1 from LUMINOVA PHARMA GROUP (Guatemala) on Oct 21, 2026. The refused product falls under Drugs and Biologics — AMOXICILLIN TRIHYDRATE (PENICILLIN, SYNTHETICALLY PRODUCED). Cited charge: 75 This firm has 4 other import refusals on record.

Refusal details

Date
Oct 21, 2026
Country
Guatemala
Product Category
Drugs and Biologics
Product Code
56BCY03 AMOXICILLIN TRIHYDRATE (PENICILLIN, SYNTHETICALLY PRODUCED)
Charges
75

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