FDA Import Refusal AEK-2395007-1/1/1 — Opko Instrumentation Llc
The FDA refused shipment AEK-2395007-1/1/1 from Opko Instrumentation Llc (United States) on Sep 7, 2016. The refused product falls under Devices — ULTRASOUND, SKIN PERMEATION. Cited charges: 118,16,3280,341
Refusal Details
- Date
- Sep 7, 2016
- Country
- United States
- Product Category
- Devices
- Product Code
- 79NRJ ULTRASOUND, SKIN PERMEATION
- Charges
- 118,16,3280,341