FDA Import Refusal AEK-4431765-6/11/1 — PENTASHOT EU SRO

PENTASHOT EU SRO — FEI 3012851483

The FDA refused shipment AEK-4431765-6/11/1 from PENTASHOT EU SRO (Czech Republic) on Aug 21, 2018. The refused product falls under Radiological Health — GENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL. Cited charge: 47 This firm has 1 other import refusal on record.

Refusal details

Date
Aug 21, 2018
Country
Czech Republic
Product Category
Radiological Health
Product Code
95RDW GENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
Charges
47

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