Home / Import refusals / AEK-3243934-9/81/1

FDA Import Refusal AEK-3243934-9/81/1 — Oakley Inc

Oakley Inc — FEI 2083323

The FDA refused shipment AEK-3243934-9/81/1 from Oakley Inc (United States) on May 26, 2023. The refused product falls under Devices — LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION). Cited charge: 3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
May 26, 2023
Country
United States
Product Category
Devices
Product Code
86HQG LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
Charges
3280

Other import refusals

  • 85T-0137513-6/100001/1 (Thu Jul 02 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-3256982-2/61/1 (Fri May 26 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 85T-0105770-0/31/1 (Wed Jul 07 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 791-1019288-2/21/1 (Thu Nov 30 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 791-1019288-2/11/1 (Thu Nov 30 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources