FDA Import Refusal 799-1551622-2/11/1 — Schwind Eye-Tech-Solutions GmbH & Co. KG
The FDA refused shipment 799-1551622-2/11/1 from Schwind Eye-Tech-Solutions GmbH & Co. KG (Germany) on Mar 11, 2021. The refused product falls under Devices — BLADE, KERATOME, REPROCESSED. Cited charges: 3280,341,508 This firm has 3 other import refusals on record.
Refusal details
- Date
- Mar 11, 2021
- Country
- Germany
- Product Category
- Devices
- Product Code
- 86NKY BLADE, KERATOME, REPROCESSED
- Charges
- 3280,341,508