FDA Import Refusal AEK-6334770-9/11/1 — Iridex Corporation
The FDA refused shipment AEK-6334770-9/11/1 from Iridex Corporation (United States) on October 7, 2019. The refused product falls under Devices — LASER, OPHTHALMIC. Cited charge: 47 This firm has 1 other import refusal on record.
Refusal Details
- Date
- October 7, 2019
- Country
- United States
- Product Category
- Devices
- Product Code
- 86HQF LASER, OPHTHALMIC
- Charges
- 47