FDA Import Refusal FR1-0018248-9/101/1 — AQUISEL S.L.U.
The FDA refused shipment FR1-0018248-9/101/1 from AQUISEL S.L.U. (Spain) on January 11, 2022. The refused product falls under Devices — TEST, ERYTHROCYTE SEDIMENTATION RATE. Cited charge: 118 This firm has 4 other import refusals on record.
Refusal Details
- Date
- January 11, 2022
- Country
- Spain
- Product Category
- Devices
- Product Code
- 81JPH TEST, ERYTHROCYTE SEDIMENTATION RATE
- Charges
- 118