FDA Import Refusal 799-0712472-1/11/1 — Accriva Diagnostics, Inc.
The FDA refused shipment 799-0712472-1/11/1 from Accriva Diagnostics, Inc. (United States) on Sep 22, 2022. The refused product falls under Devices — SYSTEM, AUTOMATED PLATELET AGGREGATION. Cited charges: 118,3280,341,508
Refusal Details
- Date
- Sep 22, 2022
- Country
- United States
- Product Category
- Devices
- Product Code
- 81JOZ SYSTEM, AUTOMATED PLATELET AGGREGATION
- Charges
- 118,3280,341,508