Home / Import refusals / AEK-5354644-3/21/1

FDA Import Refusal AEK-5354644-3/21/1 — Siemens Healthcare Diagnostics Inc.

Siemens Healthcare Diagnostics Inc. — FEI 1000122204

The FDA refused shipment AEK-5354644-3/21/1 from Siemens Healthcare Diagnostics Inc. (United States) on December 4, 2018. The refused product falls under Devices — RADIOIMMUNOASSAY, PARATHYROID HORMONE. 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
75CEW RADIOIMMUNOASSAY, PARATHYROID HORMONE
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