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FDA Import Refusal AEK-7103962-9/11/1 — Micobiomed Co

Micobiomed Co — FEI 3011952970

The FDA refused shipment AEK-7103962-9/11/1 from Micobiomed Co (South Korea) on May 12, 2020. The refused product falls under Devices — NON-SARS CORONAVIRUS MULTIPLEX NUCLEIC ACID ASSAY. Cited charge: 508

Refusal details

Date
May 12, 2020
Country
South Korea
Product Category
Devices
Product Code
83OTG NON-SARS CORONAVIRUS MULTIPLEX NUCLEIC ACID ASSAY
Charges
508

FDA data resources

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