FDA Import Refusal AEK-8468993-2/11/1 — SCHALCON S. P. A.
The FDA refused shipment AEK-8468993-2/11/1 from SCHALCON S. P. A. (Italy) on May 9, 2025. The refused product falls under Devices — DAILY WEAR SOFT CONTACT LENS TO REDUCE THE PROGRESSION OF MYOPIA. Cited charges: 118,3260,3280
Refusal Details
- Date
- May 9, 2025
- Country
- Italy
- Product Category
- Devices
- Product Code
- 86QIT DAILY WEAR SOFT CONTACT LENS TO REDUCE THE PROGRESSION OF MYOPIA
- Charges
- 118,3260,3280