FDA Import Refusal 201-2747714-8/1/1 — Plusoptix AG

Plusoptix AG — FEI 3003829667

The FDA refused shipment 201-2747714-8/1/1 from Plusoptix AG (Germany) on Aug 5, 2013. The refused product falls under Devices — REFRACTOMETER, OPHTHALMIC. Cited charge: 118

Refusal details

Date
Aug 5, 2013
Country
Germany
Product Category
Devices
Product Code
86HKO REFRACTOMETER, OPHTHALMIC
Charges
118

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