Home / Import refusals / 510-8221185-8/21/1

FDA Import Refusal 510-8221185-8/21/1 — FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office

FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office — FEI 3010516924

The FDA refused shipment 510-8221185-8/21/1 from FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office (Japan) on August 8, 2017. The refused product falls under Devices — COLONOSCOPE, GASTRO-UROLOGY. Cited charges: 118,3280 This firm has 3 other import refusals on record.

Refusal Details

Date
August 8, 2017
Country
Japan
Product Category
Devices
Product Code
78FDF COLONOSCOPE, GASTRO-UROLOGY
Charges
118,3280

Recent inspections

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Other import refusals

  • 799-7632322-9/11/1 (Mon Apr 11 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 510-8221185-8/31/1 (Tue Aug 08 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 510-8221185-8/11/1 (Tue Aug 08 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources