FDA Import Refusal 799-5186110-2/11/1 — Rovipharm

Rovipharm — FEI 3010894114

The FDA refused shipment 799-5186110-2/11/1 from Rovipharm (France) on Nov 10, 2021. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED. Cited charges: 118,3280,508

Refusal details

Date
Nov 10, 2021
Country
France
Product Category
Devices
Product Code
80NKK NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
Charges
118,3280,508

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