FDA Import Refusal EQ6-0009153-0/1/1 — Oculus Optikgeraete GMBH

Oculus Optikgeraete GMBH — FEI 3002807782

The FDA refused shipment EQ6-0009153-0/1/1 from Oculus Optikgeraete GMBH (Germany) on Mar 19, 2009. The refused product falls under Devices — DEVICE, GENERAL MEDICAL. Cited charges: 341,508 This firm has 1 other import refusal on record.

Refusal details

Date
Mar 19, 2009
Country
Germany
Product Category
Devices
Product Code
80LDQ DEVICE, GENERAL MEDICAL
Charges
341,508

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