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FDA Import Refusal AEK-1038197-6/11/1C — REVITACARE

REVITACARE — FEI 3018123879

The FDA refused shipment AEK-1038197-6/11/1C from REVITACARE (France) on Jul 14, 2022. 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
Jul 14, 2022
Country
France
Product Category
Devices
Product Code
87MOZ ACID, HYALURONIC, INTRAARTICULAR
Charges
118,237,3280

Other import refusals

FDA data resources

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