FDA Import Refusal FR1-0018903-9/61/1 — Kimetec Gmbh Medizintechnik

Kimetec Gmbh Medizintechnik — FEI 3008145250

The FDA refused shipment FR1-0018903-9/61/1 from Kimetec Gmbh Medizintechnik (Germany) on Jan 22, 2024. The refused product falls under Devices — TOURNIQUET, NONPNEUMATIC. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Jan 22, 2024
Country
Germany
Product Category
Devices
Product Code
79GAX TOURNIQUET, NONPNEUMATIC
Charges
118,3280

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