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FDA Import Refusal 799-1923797-3/11/1 — SPECTRUMX

SPECTRUMX — FEI 3018224124

The FDA refused shipment 799-1923797-3/11/1 from SPECTRUMX (United Kingdom) on Apr 20, 2021. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charge: 508 This firm has 1 other import refusal on record.

Refusal details

Date
Apr 20, 2021
Country
United Kingdom
Product Category
Devices
Product Code
83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Charges
508

Other import refusals

FDA data resources

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