FDA Import Refusal 799-1682760-3/11/1 — Smartway Pharmaceuticals
The FDA refused shipment 799-1682760-3/11/1 from Smartway Pharmaceuticals (United Kingdom) on Oct 28, 2022. The refused product falls under Devices — MULTIPLE USE BLOOD LANCET FOR SINGLE PATIENT USE ONLY. Cited charges: 118,3280,341,508
Refusal details
- Date
- Oct 28, 2022
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 79QRL MULTIPLE USE BLOOD LANCET FOR SINGLE PATIENT USE ONLY
- Charges
- 118,3280,341,508