FDA Import Refusal AEK-7401350-5/2/1 — Kapitex Healthcare Ltd
The FDA refused shipment AEK-7401350-5/2/1 from Kapitex Healthcare Ltd (United Kingdom) on Jun 7, 2004. The refused product falls under Devices — TUBE, LARYNGECTOMY. Cited charge: 341 This firm has 1 other import refusal on record.
Refusal details
- Date
- Jun 7, 2004
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 77KAC TUBE, LARYNGECTOMY
- Charges
- 341