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FDA Import Refusal AEK-1282205-8/1/1 — Endostim Inc

Endostim Inc — FEI 3008288566

The FDA refused shipment AEK-1282205-8/1/1 from Endostim Inc (United States) on May 5, 2014. The refused product falls under Devices — INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT. Cited charges: 118,508

Refusal Details

Date
May 5, 2014
Country
United States
Product Category
Devices
Product Code
87HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT
Charges
118,508

FDA data resources