FDA Import Refusal MC2-6188939-8/2/1 — Kontron Instruments Sa

Kontron Instruments Sa — FEI 3002807409

The FDA refused shipment MC2-6188939-8/2/1 from Kontron Instruments Sa (France) on Jun 24, 2010. The refused product falls under Devices — SYSTEM, IMAGING, PULSED ECHO, ULTRASONIC. Cited charges: 118,341 This firm has 1 other import refusal on record.

Refusal details

Date
Jun 24, 2010
Country
France
Product Category
Devices
Product Code
90IYO SYSTEM, IMAGING, PULSED ECHO, ULTRASONIC
Charges
118,341

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