FDA Import Refusal AEK-8458385-2/11/1 — Boditech Med, Inc.
The FDA refused shipment AEK-8458385-2/11/1 from Boditech Med, Inc. (South Korea) on Dec 19, 2021. The refused product falls under Devices — KIT, ASSAY, PROGESTERONE RECEPTOR. Cited charges: 118,237,3280 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Dec 19, 2021
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 75LPI KIT, ASSAY, PROGESTERONE RECEPTOR
- Charges
- 118,237,3280