FDA Import Refusal AEK-0543713-1/10002/1 — Penlon Limited
The FDA refused shipment AEK-0543713-1/10002/1 from Penlon Limited (United Kingdom) on Jun 10, 2026. The refused product falls under Devices — VAPORIZER, ANESTHESIA, NON-HEATED. Cited charge: 341 This firm has 1 other import refusal on record.
Refusal details
- Date
- Jun 10, 2026
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 73CAD VAPORIZER, ANESTHESIA, NON-HEATED
- Charges
- 341