FDA Import Refusal AEK-1704667-1/61/1 — Gebruder Brasseler GmbH & Co. KG

Gebruder Brasseler GmbH & Co. KG — FEI 3002806577

The FDA refused shipment AEK-1704667-1/61/1 from Gebruder Brasseler GmbH & Co. KG (Germany) on Sep 30, 2022. The refused product falls under Devices — BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL. Cited charge: 3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Sep 30, 2022
Country
Germany
Product Category
Devices
Product Code
79GFA BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL
Charges
3280

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