FDA Import Refusal AEK-0510868-1/31/1 — Boditech Med, Inc.
The FDA refused shipment AEK-0510868-1/31/1 from Boditech Med, Inc. (South Korea) on Mar 12, 2022. The refused product falls under Devices — KIT, TEST, PREGNANCY, HCG, OVER THE COUNTER. Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Mar 12, 2022
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 75LCX KIT, TEST, PREGNANCY, HCG, OVER THE COUNTER
- Charges
- 118,3280,508