FDA Import Refusal 799-9342434-7/21/2 — Kimberly-Clark Corporation

Kimberly-Clark Corporation — FEI 1000015879

The FDA refused shipment 799-9342434-7/21/2 from Kimberly-Clark Corporation (United States) on December 17, 2018. The refused product falls under Devices — GLOVE, PATIENT EXAMINATION. Cited charge: 118 This firm has 3 other import refusals on record.

Refusal Details

Date
December 17, 2018
Country
United States
Product Category
Devices
Product Code
80FMC GLOVE, PATIENT EXAMINATION
Charges
118