FDA Import Refusal 799-1726994-4/11/1 — Kmt Kuelzer Medizintechnik Gmbh

Kmt Kuelzer Medizintechnik Gmbh — FEI 3006749182

The FDA refused shipment 799-1726994-4/11/1 from Kmt Kuelzer Medizintechnik Gmbh (Germany) on Jun 6, 2019. The refused product falls under Devices — TRANSDUCER, ULTRASONIC, DIAGNOSTIC. Cited charges: 118,3280 This firm has 1 other import refusal on record.

Refusal details

Date
Jun 6, 2019
Country
Germany
Product Category
Devices
Product Code
90ITX TRANSDUCER, ULTRASONIC, DIAGNOSTIC
Charges
118,3280

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