FDA Import Refusal 1FX-4289807-3/10001/1 — Bausch & Lomb Incorporated
The FDA refused shipment 1FX-4289807-3/10001/1 from Bausch & Lomb Incorporated (United States) on Sep 18, 2026. The refused product falls under Devices — DAILY WEAR SOFT CONTACT LENS TO REDUCE THE PROGRESSION OF MYOPIA. Cited charge: 118 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Sep 18, 2026
- Country
- United States
- Product Category
- Devices
- Product Code
- 86QIT DAILY WEAR SOFT CONTACT LENS TO REDUCE THE PROGRESSION OF MYOPIA
- Charges
- 118