FDA Import Refusal 799-7775487-8/21/1 — MJK INSTRUMENTS

MJK INSTRUMENTS — FEI 3024226185

The FDA refused shipment 799-7775487-8/21/1 from MJK INSTRUMENTS (France) on Nov 2, 2023. The refused product falls under Devices — BLADE, SCALPEL. Cited charges: 118,3280 This firm has 2 other import refusals on record.

Refusal Details

Date
Nov 2, 2023
Country
France
Product Category
Devices
Product Code
79GES BLADE, SCALPEL
Charges
118,3280

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