FDA Import Refusal AEK-1924010-7/1/1 — Artron Laboratories, Inc.
The FDA refused shipment AEK-1924010-7/1/1 from Artron Laboratories, Inc. (Canada) on Apr 21, 2016. The refused product falls under Devices — TEST, HIV DETECTION. Cited charges: 118,237 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Apr 21, 2016
- Country
- Canada
- Product Category
- Devices
- Product Code
- 82MZF TEST, HIV DETECTION
- Charges
- 118,237