FDA Import Refusal AEK-1135368-3/1/1 — Technolas Perfect Vision GmbH
The FDA refused shipment AEK-1135368-3/1/1 from Technolas Perfect Vision GmbH (Germany) on May 10, 2013. The refused product falls under Devices — KERATOME, AC-POWERED. Cited charges: 118,3280,341
Refusal details
- Date
- May 10, 2013
- Country
- Germany
- Product Category
- Devices
- Product Code
- 86HNO KERATOME, AC-POWERED
- Charges
- 118,3280,341