FDA Import Refusal 112-8913045-5/4/1 — Owen Mumfordltd.
The FDA refused shipment 112-8913045-5/4/1 from Owen Mumfordltd. (United Kingdom) on January 31, 2011. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charge: 118 This firm has 1 other import refusal on record.
Refusal Details
- Date
- January 31, 2011
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
- Charges
- 118