FDA Import Refusal 231-9566167-7/1/1 — Johnson & Johnson
The FDA refused shipment 231-9566167-7/1/1 from Johnson & Johnson (Brazil) on Jun 1, 2015. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charge: 118 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Jun 1, 2015
- Country
- Brazil
- Product Category
- Devices
- Product Code
- 79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
- Charges
- 118