FDA Import Refusal 799-1453182-7/11/1 — Cooper Vision

Cooper Vision — FEI 3004510061

The FDA refused shipment 799-1453182-7/11/1 from Cooper Vision (United Kingdom) on Nov 2, 2022. The refused product falls under Devices — DAILY WEAR SOFT CONTACT LENS TO REDUCE THE PROGRESSION OF MYOPIA. Cited charge: 82 This firm has 5 or more other import refusals on record.

Refusal details

Date
Nov 2, 2022
Country
United Kingdom
Product Category
Devices
Product Code
86QIT DAILY WEAR SOFT CONTACT LENS TO REDUCE THE PROGRESSION OF MYOPIA
Charges
82

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.