FDA Import Refusal FR1-0018508-6/71/1 — AQUISEL S.L.U.
The FDA refused shipment FR1-0018508-6/71/1 from AQUISEL S.L.U. (Spain) on August 3, 2022. The refused product falls under Devices — TEST, ERYTHROCYTE SEDIMENTATION RATE. Cited charge: 508 This firm has 4 other import refusals on record.
Refusal Details
- Date
- August 3, 2022
- Country
- Spain
- Product Category
- Devices
- Product Code
- 81JPH TEST, ERYTHROCYTE SEDIMENTATION RATE
- Charges
- 508