FDA Import Refusal 799-3233041-8/11/1 — Mediproma B.V.

Mediproma B.V. — FEI 3011118388

The FDA refused shipment 799-3233041-8/11/1 from Mediproma B.V. (Netherlands) on Feb 21, 2023. The refused product falls under Devices — SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC. Cited charges: 118,3280,508 This firm has 3 other import refusals on record.

Refusal Details

Date
Feb 21, 2023
Country
Netherlands
Product Category
Devices
Product Code
90IYN SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC
Charges
118,3280,508

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