FDA Import Refusal AEK-8091213-9/31/1 — Paradigm Spine Gmbh
The FDA refused shipment AEK-8091213-9/31/1 from Paradigm Spine Gmbh (Germany) on Nov 25, 2020. The refused product falls under Devices — ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE. Cited charges: 118,3280,341 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Nov 25, 2020
- Country
- Germany
- Product Category
- Devices
- Product Code
- 87NKB ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE
- Charges
- 118,3280,341