FDA Import Refusal AEK-5607084-7/11/1 — Hansaton Akustik Gmbh

Hansaton Akustik Gmbh — FEI 3010299075

The FDA refused shipment AEK-5607084-7/11/1 from Hansaton Akustik Gmbh (Germany) on Feb 26, 2019. The refused product falls under Devices — MASKER, TINNITIS. Cited charges: 118,3280 This firm has 1 other import refusal on record.

Refusal details

Date
Feb 26, 2019
Country
Germany
Product Category
Devices
Product Code
77KLW MASKER, TINNITIS
Charges
118,3280

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