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FDA Import Refusal 112-3382817-2/1/1 — Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. — FEI 2432235

The FDA refused shipment 112-3382817-2/1/1 from Siemens Healthcare Diagnostics, Inc. (United States) on September 1, 2011. The refused product falls under Drugs and Biologics — ANTIHEMOPHILIC FACTOR. Cited charge: 179 This firm has 5 or more other import refusals on record.

Refusal Details

Date
September 1, 2011
Country
United States
Product Category
Drugs and Biologics
Product Code
57UH02 ANTIHEMOPHILIC FACTOR
Charges
179

Recent inspections

  • 1230618 (NAI Fri May 24 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1167476 (NAI Wed Mar 30 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1141620 (NAI Fri Mar 12 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1012263 (VAI Wed May 31 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 896868 (NAI Fri Sep 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

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