FDA Import Refusal 101-5957433-4/11/1 — MEKO LASER MATERIAL PROCESSING
The FDA refused shipment 101-5957433-4/11/1 from MEKO LASER MATERIAL PROCESSING (Germany) on Jun 5, 2019. The refused product falls under Devices — ANGIOGRAPHY/ANGIOPLASTY KIT. Cited charge: 508 This firm has 1 other import refusal on record.
Refusal details
- Date
- Jun 5, 2019
- Country
- Germany
- Product Category
- Devices
- Product Code
- 74OEQ ANGIOGRAPHY/ANGIOPLASTY KIT
- Charges
- 508