FDA Import Refusal AEK-9455311-0/10002/1 — Dca Design Consultants Ltd
The FDA refused shipment AEK-9455311-0/10002/1 from Dca Design Consultants Ltd (United Kingdom) on May 29, 2026. The refused product falls under Devices — ACTUATOR, SYRINGE, INJECTOR TYPE. Cited charges: 118,3280,341,508
Refusal Details
- Date
- May 29, 2026
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 80DQF ACTUATOR, SYRINGE, INJECTOR TYPE
- Charges
- 118,3280,341,508