FDA Import Refusal 799-7219208-1/11/1 — INSTRON GMBH
The FDA refused shipment 799-7219208-1/11/1 from INSTRON GMBH (Germany) on Feb 10, 2022. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charge: 508
Refusal details
- Date
- Feb 10, 2022
- Country
- Germany
- Product Category
- Devices
- Product Code
- 83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
- Charges
- 508