FDA Import Refusal AEK-2871301-1/11/1 — REPROLIFE INC
The FDA refused shipment AEK-2871301-1/11/1 from REPROLIFE INC (Japan) on Jan 13, 2017. The refused product falls under Devices — LABWARE, ASSISTED REPRODUCTION. Cited charges: 118,3280,508
Refusal details
- Date
- Jan 13, 2017
- Country
- Japan
- Product Category
- Devices
- Product Code
- 85MQK LABWARE, ASSISTED REPRODUCTION
- Charges
- 118,3280,508