FDA Import Refusal 799-9571120-6/11/1 — INTECH EUROPE
The FDA refused shipment 799-9571120-6/11/1 from INTECH EUROPE (France) on Jul 13, 2022. The refused product falls under Devices — INSTRUMENT, MANUAL, GENERAL SURGICAL. Cited charges: 118,3280,508
Refusal details
- Date
- Jul 13, 2022
- Country
- France
- Product Category
- Devices
- Product Code
- 79MDM INSTRUMENT, MANUAL, GENERAL SURGICAL
- Charges
- 118,3280,508