FDA Import Refusal 799-6469245-3/51/1 — REVITACARE

REVITACARE — FEI 3018123879

The FDA refused shipment 799-6469245-3/51/1 from REVITACARE (France) on Aug 15, 2023. The refused product falls under Devices — ACID, HYALURONIC, INTRAARTICULAR. Cited charges: 118,237,3280 This firm has 4 other import refusals on record.

Refusal Details

Date
Aug 15, 2023
Country
France
Product Category
Devices
Product Code
87MOZ ACID, HYALURONIC, INTRAARTICULAR
Charges
118,237,3280

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