Home / Import refusals / HK8-5301847-9/11/1

FDA Import Refusal HK8-5301847-9/11/1 — OMNI LENS PVT. LTD.

OMNI LENS PVT. LTD. — FEI 3008449456

The FDA refused shipment HK8-5301847-9/11/1 from OMNI LENS PVT. LTD. (India) on December 30, 2020. The refused product falls under Devices — LENS, INTRAOCULAR. Cited charge: 237 This firm has 3 other import refusals on record.

Refusal Details

Date
December 30, 2020
Country
India
Product Category
Devices
Product Code
86HQL LENS, INTRAOCULAR
Charges
237

Recent inspections

  • 1279741 (VAI Thu Jul 10 2025 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • HK8-5300472-7/11/1 (Fri Jan 31 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • HK8-5301274-6/11/1 (Fri Jan 31 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • HK8-5302076-4/11/1 (Fri Jan 31 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources