FDA Import Refusal D99-1433456-9/11/1A — Angiplast Private Limited

Angiplast Private Limited — FEI 3003348363

The FDA refused shipment D99-1433456-9/11/1A from Angiplast Private Limited (India) on July 3, 2019. The refused product falls under Devices — SET, I.V. FLUID TRANSER. Cited charge: 2780 This firm has 4 other import refusals on record.

Refusal Details

Date
July 3, 2019
Country
India
Product Category
Devices
Product Code
80LHI SET, I.V. FLUID TRANSER
Charges
2780