FDA Import Refusal AEK-4305130-6/11/1 — PENTASHOT EU SRO
The FDA refused shipment AEK-4305130-6/11/1 from PENTASHOT EU SRO (Czech Republic) on Mar 14, 2018. The refused product falls under Radiological Health — GENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL. Cited charge: 476 This firm has 1 other import refusal on record.
Refusal details
- Date
- Mar 14, 2018
- Country
- Czech Republic
- Product Category
- Radiological Health
- Product Code
- 95RDW GENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
- Charges
- 476