FDA Import Refusal 799-2962187-8/21/1 — Oscor Inc.

Oscor Inc. — FEI 1035166

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