FDA Import Refusal AEK-9798866-7/2/1 — ANSELL N.P. SDN. BHD.

ANSELL N.P. SDN. BHD. — FEI 3003221560

The FDA refused shipment AEK-9798866-7/2/1 from ANSELL N.P. SDN. BHD. (Malaysia) on June 22, 2009. The refused product falls under Devices — GLOVE, PATIENT EXAMINATION, LATEX. Cited charges: 341,508 This firm has 3 other import refusals on record.

Refusal Details

Date
June 22, 2009
Country
Malaysia
Product Category
Devices
Product Code
80LYY GLOVE, PATIENT EXAMINATION, LATEX
Charges
341,508