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FDA Import Refusal 799-0687551-3/11/1 — NDI Europe GmbH

NDI Europe GmbH — FEI 3008301410

The FDA refused shipment 799-0687551-3/11/1 from NDI Europe GmbH (Germany) on Sep 22, 2022. The refused product falls under Devices — DEVICE, THERMAL ABLATION, ENDOMETRIAL. Cited charge: 237 This firm has 3 other import refusals on record.

Refusal details

Date
Sep 22, 2022
Country
Germany
Product Category
Devices
Product Code
85MNB DEVICE, THERMAL ABLATION, ENDOMETRIAL
Charges
237

Other import refusals

FDA data resources

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