FDA Import Refusal 112-5921999-1/1/1 — Schwind Eye-Tech-Solutions GmbH & Co. KG
The FDA refused shipment 112-5921999-1/1/1 from Schwind Eye-Tech-Solutions GmbH & Co. KG (Germany) on Mar 14, 2012. The refused product falls under Devices — KERATOME, AC-POWERED. Cited charges: 118,508 This firm has 3 other import refusals on record.
Refusal details
- Date
- Mar 14, 2012
- Country
- Germany
- Product Category
- Devices
- Product Code
- 86HNO KERATOME, AC-POWERED
- Charges
- 118,508