Home / Import refusals / F23-9072512-5/1/1

FDA Import Refusal F23-9072512-5/1/1 — Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. — FEI 2432235

The FDA refused shipment F23-9072512-5/1/1 from Siemens Healthcare Diagnostics, Inc. (United States) on December 6, 2012. The refused product falls under Devices — URINE COLLECTION KIT (EXCLUDES HIV TESTING). Cited charges: 118,341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
December 6, 2012
Country
United States
Product Category
Devices
Product Code
75OIE URINE COLLECTION KIT (EXCLUDES HIV TESTING)
Charges
118,341

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