FDA Import Refusal M21-0722722-7/1/1 — Arrow International, Inc. (Subsidiary of Teleflex, Inc.)

Arrow International, Inc. (Subsidiary of Teleflex, Inc.) — FEI 3015859709

The FDA refused shipment M21-0722722-7/1/1 from Arrow International, Inc. (Subsidiary of Teleflex, Inc.) (United States) on February 26, 2002. The refused product falls under Devices — CATHETER, INTRAVASCULAR, DIAGNOSTIC. Cited charges: 118,341,508

Refusal Details

Date
February 26, 2002
Country
United States
Product Category
Devices
Product Code
74DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC
Charges
118,341,508