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FDA Import Refusal AEK-5354644-3/41/1 — Siemens Healthcare Diagnostics Inc.

Siemens Healthcare Diagnostics Inc. — FEI 1000122204

The FDA refused shipment AEK-5354644-3/41/1 from Siemens Healthcare Diagnostics Inc. (United States) on December 4, 2018. The refused product falls under Devices — ANALYZER, CHEMISTRY (PHOTOMETRIC, DISCRETE) FOR CLINICAL USE. Cited charges: 16,479 This firm has 5 or more other import refusals on record.

Refusal Details

Date
December 4, 2018
Country
United States
Product Category
Devices
Product Code
75JJE ANALYZER, CHEMISTRY (PHOTOMETRIC, DISCRETE) FOR CLINICAL USE
Charges
16,479

Recent inspections

  • 1030244 (NAI Tue Sep 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • AEK-5354644-3/101/1 (Tue Dec 04 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-5354644-3/61/1 (Tue Dec 04 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-5354644-3/121/1 (Tue Dec 04 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-5354644-3/51/1 (Tue Dec 04 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-5354644-3/81/1 (Tue Dec 04 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources