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FDA Import Refusal 110-4818394-3/1/1 — Ortho-Clinical Diagnostics

Ortho-Clinical Diagnostics — FEI 3003722914

The FDA refused shipment 110-4818394-3/1/1 from Ortho-Clinical Diagnostics (United Kingdom) on Feb 12, 2004. The refused product falls under Devices — KIT, TEST, ALPHA-FETOPROTEIN FOR NEURAL TUBE DEFECTS. Cited charges: 118,508 This firm has 2 other import refusals on record.

Refusal details

Date
Feb 12, 2004
Country
United Kingdom
Product Category
Devices
Product Code
82LOK KIT, TEST, ALPHA-FETOPROTEIN FOR NEURAL TUBE DEFECTS
Charges
118,508

Other import refusals

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.