FDA Import Refusal AEK-3867250-4/51/1 — Kazu Planning Inc.
The FDA refused shipment AEK-3867250-4/51/1 from Kazu Planning Inc. (Japan) on Oct 23, 2017. The refused product falls under Devices — SUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE). Cited charge: 235 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Oct 23, 2017
- Country
- Japan
- Product Category
- Devices
- Product Code
- 86HQY SUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
- Charges
- 235