FDA Import Refusal AEK-5020222-3/11/1 — Lawrence & Mayo
The FDA refused shipment AEK-5020222-3/11/1 from Lawrence & Mayo (India) on Apr 11, 2024. The refused product falls under Devices — LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION). Cited charges: 118,3280,508
Refusal Details
- Date
- Apr 11, 2024
- Country
- India
- Product Category
- Devices
- Product Code
- 86HQG LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
- Charges
- 118,3280,508