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FDA Import Refusal 799-8951082-8/11/1 — Modality Group Ltd

Modality Group Ltd — FEI 3013204397

The FDA refused shipment 799-8951082-8/11/1 from Modality Group Ltd (United Kingdom) on Jan 3, 2019. The refused product falls under Devices — TRANSDUCER, ULTRASONIC, DIAGNOSTIC. Cited charges: 118,508

Refusal details

Date
Jan 3, 2019
Country
United Kingdom
Product Category
Devices
Product Code
90ITX TRANSDUCER, ULTRASONIC, DIAGNOSTIC
Charges
118,508

FDA data resources

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