FDA Import Refusal AEK-7081983-1/11/1 — Artron Laboratories, Inc.
The FDA refused shipment AEK-7081983-1/11/1 from Artron Laboratories, Inc. (Canada) on May 6, 2020. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charges: 336,508 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- May 6, 2020
- Country
- Canada
- Product Category
- Devices
- Product Code
- 83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
- Charges
- 336,508