FDA Import Refusal 799-2962187-8/21/1 — Oscor Inc.
The FDA refused shipment 799-2962187-8/21/1 from Oscor Inc. (United States) on March 29, 2023. The refused product falls under Devices — STIMULATOR, NEUROMUSCULAR, LOWER BACK MUSCLES, TOTALLY IMPLANTED FOR PAIN RELIEF. Cited charge: 341 This firm has 3 other import refusals on record.
Refusal Details
- Date
- March 29, 2023
- Country
- United States
- Product Category
- Devices
- Product Code
- 84QLK STIMULATOR, NEUROMUSCULAR, LOWER BACK MUSCLES, TOTALLY IMPLANTED FOR PAIN RELIEF
- Charges
- 341