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