FDA Import Refusal AEK-8664789-5/11/1 — Medtronic Inc
The FDA refused shipment AEK-8664789-5/11/1 from Medtronic Inc (United States) on Jan 5, 2021. The refused product falls under Devices — DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Jan 5, 2021
- Country
- United States
- Product Category
- Devices
- Product Code
- 79GEI DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
- Charges
- 118,3280