FDA Import Refusal 112-1170768-3/1/1 — Portex Ltd
The FDA refused shipment 112-1170768-3/1/1 from Portex Ltd (United Kingdom) on Nov 22, 2002. The refused product falls under Devices — CATHETER, BALLOON TYPE. Cited charge: 508 This firm has 1 other import refusal on record.
Refusal details
- Date
- Nov 22, 2002
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 79GBA CATHETER, BALLOON TYPE
- Charges
- 508