FDA Import Refusal CDF-0347347-0/51/1 — Agupunt S.L.

Agupunt S.L. — FEI 3011541120

The FDA refused shipment CDF-0347347-0/51/1 from Agupunt S.L. (Spain) on August 27, 2020. The refused product falls under Devices — NEEDLE, ACUPUNCTURE, SINGLE USE. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
August 27, 2020
Country
Spain
Product Category
Devices
Product Code
80MQX NEEDLE, ACUPUNCTURE, SINGLE USE
Charges
118,3280