FDA Import Refusal AEK-0879013-9/11/1 — Boditech Med, Inc.
The FDA refused shipment AEK-0879013-9/11/1 from Boditech Med, Inc. (South Korea) on Apr 7, 2022. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charge: 508 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Apr 7, 2022
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
- Charges
- 508