FDA Import Refusal 799-6673396-3/11/1 — RDT
The FDA refused shipment 799-6673396-3/11/1 from RDT (United Kingdom) on Jul 6, 2018. 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
- Jul 6, 2018
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
- Charges
- 118