FDA Import Refusal 799-5832566-9/1/1 — OKO SOLUTION S.A.S.

OKO SOLUTION S.A.S. — FEI 3009385312

The FDA refused shipment 799-5832566-9/1/1 from OKO SOLUTION S.A.S. (France) on Sep 1, 2016. The refused product falls under Devices — COMPONENT, EXTERNAL, LIMB, ANKLE/FOOT. Cited charges: 118,3280

Refusal details

Date
Sep 1, 2016
Country
France
Product Category
Devices
Product Code
89ISH COMPONENT, EXTERNAL, LIMB, ANKLE/FOOT
Charges
118,3280

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