FDA Import Refusal 799-3351520-4/61/1 — Kazu Planning Inc.

Kazu Planning Inc. — FEI 3003304449

The FDA refused shipment 799-3351520-4/61/1 from Kazu Planning Inc. (Japan) on Dec 15, 2017. 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
Dec 15, 2017
Country
Japan
Product Category
Devices
Product Code
86HQG LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
Charges
3280

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.