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FDA Import Refusal H77-0208448-1/11/3 — ARCERA GMBH

ARCERA GMBH — FEI 3015373820

The FDA refused shipment H77-0208448-1/11/3 from ARCERA GMBH (Germany) on Mar 23, 2023. The refused product falls under Devices — ACID, HYALURONIC, INTRAARTICULAR. Cited charge: 223 This firm has 5 or more other import refusals on record.

Refusal details

Date
Mar 23, 2023
Country
Germany
Product Category
Devices
Product Code
87MOZ ACID, HYALURONIC, INTRAARTICULAR
Charges
223

Other import refusals

FDA data resources

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