FDA Import Refusal 202-2916708-3/1/1 — Oculus Optikgeraete GMBH

Oculus Optikgeraete GMBH — FEI 3002807782

The FDA refused shipment 202-2916708-3/1/1 from Oculus Optikgeraete GMBH (Germany) on Sep 25, 2015. The refused product falls under Devices — DEVICE, STORAGE, IMAGES, OPHTHALMIC. Cited charges: 118,508 This firm has 1 other import refusal on record.

Refusal details

Date
Sep 25, 2015
Country
Germany
Product Category
Devices
Product Code
86NFF DEVICE, STORAGE, IMAGES, OPHTHALMIC
Charges
118,508

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