FDA Import Refusal 799-9639032-2/11/1 — ENERGIST LTD
The FDA refused shipment 799-9639032-2/11/1 from ENERGIST LTD (United Kingdom) on Jan 29, 2021. The refused product falls under Devices — PEDICLE SCREW SPINAL SYSTEM, ADOLESCENT IDIOPATHIC SCOLIOSIS. Cited charge: 341
Refusal details
- Date
- Jan 29, 2021
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 87OSH PEDICLE SCREW SPINAL SYSTEM, ADOLESCENT IDIOPATHIC SCOLIOSIS
- Charges
- 341