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FDA Import Refusal AEK-1645874-5/11/1 — FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa

FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa — FEI 3018423337

The FDA refused shipment AEK-1645874-5/11/1 from FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa (Japan) on Sep 26, 2022. The refused product falls under Devices — TRANSDUCER, ULTRASONIC, DIAGNOSTIC. Cited charges: 118,3280,341,508

Refusal details

Date
Sep 26, 2022
Country
Japan
Product Category
Devices
Product Code
90ITX TRANSDUCER, ULTRASONIC, DIAGNOSTIC
Charges
118,3280,341,508

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