Home / Import refusals / AEK-0543713-1/10002/1

FDA Import Refusal AEK-0543713-1/10002/1 — Penlon Limited

Penlon Limited — FEI 3002807907

The FDA refused shipment AEK-0543713-1/10002/1 from Penlon Limited (United Kingdom) on June 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
June 10, 2026
Country
United Kingdom
Product Category
Devices
Product Code
73CAD VAPORIZER, ANESTHESIA, NON-HEATED
Charges
341

Recent inspections

  • 1258262 (NAI Thu Dec 12 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1178449 (VAI Thu Jul 14 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1065790 (VAI Thu Sep 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 737706 (NAI Thu Jul 28 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 112-9047889-4/1/1 (Tue Nov 09 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources