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FDA Import Refusal AEK-5882802-8/11/1 — Qisda Corporation

Qisda Corporation — FEI 3006492307

The FDA refused shipment AEK-5882802-8/11/1 from Qisda Corporation (Taiwan) on May 10, 2019. The refused product falls under Devices — SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC. Cited charges: 118,3280 This firm has 1 other import refusal on record.

Refusal details

Date
May 10, 2019
Country
Taiwan
Product Category
Devices
Product Code
90IYN SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC
Charges
118,3280

Other import refusals

FDA data resources

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