FDA Import Refusal 799-9059433-3/21/1 — Injeflex
The FDA refused shipment 799-9059433-3/21/1 from Injeflex (Brazil) on Dec 3, 2020. The refused product falls under Devices — DEVICE, INTRAUTERINE, CONTRACEPTIVE AND INTRODUCER. Cited charge: 118
Refusal details
- Date
- Dec 3, 2020
- Country
- Brazil
- Product Category
- Devices
- Product Code
- 85HDT DEVICE, INTRAUTERINE, CONTRACEPTIVE AND INTRODUCER
- Charges
- 118