FDA Import Refusal 799-2861802-2/11/1 — AKRA DERMO JET

AKRA DERMO JET — FEI 3012703563

The FDA refused shipment 799-2861802-2/11/1 from AKRA DERMO JET (France) on Oct 15, 2019. The refused product falls under Devices — INJECTOR, FLUID, NON-ELECTRICALLY POWERED. Cited charge: 118

Refusal details

Date
Oct 15, 2019
Country
France
Product Category
Devices
Product Code
80KZE INJECTOR, FLUID, NON-ELECTRICALLY POWERED
Charges
118

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