FDA Import Refusal 799-1129397-3/11/1 — BD
The FDA refused shipment 799-1129397-3/11/1 from BD (Canada) on Apr 26, 2019. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Apr 26, 2019
- Country
- Canada
- Product Category
- Devices
- Product Code
- 79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
- Charges
- 118,3280