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FDA Import Refusal 261-0367051-4/11/1 — Moeller Medical GmbH

Moeller Medical GmbH — FEI 3002807634

The FDA refused shipment 261-0367051-4/11/1 from Moeller Medical GmbH (Germany) on May 26, 2017. The refused product falls under Devices — ELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH. Cited charge: 118

Refusal Details

Date
May 26, 2017
Country
Germany
Product Category
Devices
Product Code
89IKT ELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH
Charges
118

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