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FDA Import Refusal 231-8276654-8/81/1 — Echonous Inc

Echonous Inc — FEI 3013757696

The FDA refused shipment 231-8276654-8/81/1 from Echonous Inc (United States) on Aug 2, 2019. The refused product falls under Devices — MONITOR, ULTRASONIC, NONFETAL. Cited charge: 118 This firm has 2 other import refusals on record.

Refusal details

Date
Aug 2, 2019
Country
United States
Product Category
Devices
Product Code
90JAF MONITOR, ULTRASONIC, NONFETAL
Charges
118

Other import refusals

FDA data resources

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